Frontage is a CRO providing integrated, scientifically-driven research, analytical and product development services throughout the drug discovery and development process to enable biopharmaceutical companies to achieve their drug development goals. We are focused on helping our client’s to address their most significant and complex drug discovery and development challenges. Our scientific knowledge base, technical expertise and reputation for high quality services have been integral to our ability to turn our services into your solutions.
ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organisations. We develop new innovations, drive emerging therapies forward and improve patient lives. With headquarters in Dublin, Ireland, ICON employed approximately 41,150 employees in 113 locations in 53 countries as at September 30, 2022.
PCM Trials has been at the forefront of decentralized clinical research since 2008, leading mobile visits and recently introducing community-based research sites. We are driving the shift to patient-centric clinical trials, giving individuals the flexibility to engage in research studies in ways that work best for them. Our approach expands opportunities for participation, resulting in greater patient diversity, reduced patient dropout, and faster study results.
Worldwide is changing how the world experiences CROs – in the best possible way. From early phase, bioanalytical sciences, late phase, post-approval and real-world evidence, Worldwide Clinical Trials provides full-service drug development services for central nervous system, cardiovascular, metabolic, general medicine, oncology and rare disease therapies.
ACM Global Laboratories is one of the largest global independent central labs in the industry. ACM is certified by the College of American Pathologists (CAP) and the Substance Abuse and Mental Health Services Administration (SAMHSA). The company delivers high-quality laboratory testing and diagnostic lab services in support of both clinical trials research, toxicology and individual patient care. ACM provides a powerful combination of operational excellence, scientific expertise and unsurpassed global service to customers in more than 65 countries. ACM performs more than 20 million laboratory tests each year—spanning all medical disciplines including pathology, microbiology, molecular diagnostics, toxicology and more.
Advanced Clinical is a global clinical research services organization, providing CRO, FSP, Strategic Resourcing and Consulting Services for biopharmaceutical and medical device organizations. Our company is committed to improving all lives touched by clinical research and we address the hopes of patients and healthcare professionals with industry-leading services and technology in life sciences. Visit our website to learn more about how we deliver a Better Clinical Experience.
The Almac Group is an established contract development and manufacturing organisation providing an extensive range of integrated services across the drug development lifecycle to the pharmaceutical and biotech sectors globally.
Its innovative services range from R&D, biomarker discovery development and commercialisation, API manufacture, formulation development, clinical trial supply, IRT (IVRS/IWRS) through to commercial-scale manufacture.
The international company is a privately owned organisation which has grown organically over the past five decades now employing over 5,600 highly skilled personnel across 18 facilities including Europe, the US and Asia.
The company has a global reputation for excellence built over 50 years of client service, delivering expertise right across the drug development lifecycle and offering a tailored solution to each of our clients.
To keep up to date with latest news, follow Almac Group on Twitter and LinkedIn or visit almacgroup.com.
To learn more, please visit our website - atreo.io
Next Sponsor
Back
Company Information
BSI Life Sciences offers smart eClinical software for CTMS, eTMF and more. BSI makes life science software for people – and has done so for over 25 years. BSI’s software solution is made in Switzerland, Germany, USA and anywhere else clients need to be, and focused on being innovative and user-friendly. They focus on staying ahead of the industry trends and delivering a functional, compliant, and leading edge eClinical solution. This way, BSI helps its customers continuously optimize and accelerate the clinical development process. And that’s what they love! www.bsi-lifesciences.com
With over 40 years’ experience, 600 beds and locations in NA, EU and Asia, Celerion conducts First-in-Human, clinical Proof-of-Concept and patient dose response studies, cardiovascular safety and NDA-enabling clinical pharmacology research. Celerion provides full study services including statistics, data management and biostatistics (including PK/PD analysis), and bioanalytical services.
LabConnect is the world’s most agile central laboratory solutions partner supporting clinical trials of all sizes and complexity. With modern operations and strategic alliances with world-leading laboratories, LabConnect is uniquely positioned to provide access to the latest innovation and automation. LabConnect is the trusted partner for biotechnology, pharmaceutical, and clinical research organizations.
MedNet is a leading eClinical technology company specializing in electronic data capture and clinical study management systems. Since 2001, MedNet’s proven cloud-based solutions have successfully supported research initiatives worldwide. Visit our booth to see iMedNet eClinical…an agile, efficient and, effective solution that allows sponsors and CROs to easily build studies.
Miller Tanner Associates is a WBENC-certified, full-service global corporate event planning company specializing in the life sciences industry for 26+ years (15+ in virtual events). We deliver exceptional experiences for face-to-face, virtual, and hybrid meetings and events as well as tailored event management technology solutions including proprietary tools – EPIC™, Attend™, and VALTs™. We offer a broad spectrum of products and services to support event planning needs, including security and compliance (21CFR Part 11), engagement strategies, technology support, robust pre- and post-event reporting, and more. To learn more about Miller Tanner Associates, visit https://www.millertanner.com/
Myonex provides tailored services and solutions to advance medicine through clinical to commercial stages with tailored drug sourcing and ancillary supply, to packaging, labeling, and distribution. With ten global locations, we offer flexible, efficient, and cost-effective support for clients across the pharmaceutical and biotech sectors.
Company Website
To learn more, please visit our website - www.myonex.com
Next Sponsor
Back
Company Information
Prevail InfoWorks improves the probability of clinical trial success by providing stakeholders real-time actionable intelligence to effectively manage endpoints and key deliverables with the Single Interface™, its patented cloud-based tool that aggregates, reconciles, analyzes and single-view reports/visualizes all clinical, operational and project accounting data, regardless of the source or format.
Versiti Clinical Trials Services support biopharma and cell therapy companies through central laboratory, logistics, biomaterials provision, and IRB services. We offer customizable specimen collection kits, specialty testing capabilities, dedicated project management and trial site support, biostorage, and real-time data management and reporting. Our Leukopaks are available for Research Use Only and Clinical Grade (FDA 21 CFR 1271-compliant) applications.
Founded in 2005, Inspire connects life sciences organizations with the voices that matter most—patients and caregivers. With 10 million unique annual visitors across over 3,000 disease states, Inspire leverages its engaged patient communities to accelerate clinical trial recruitment, uncover real-world evidence, deliver actionable market research, and provide targeted advertising solutions for health-focused audiences. By bridging the gap between patients and life sciences, Inspire enables smarter decision-making and a deeper understanding of the communities it serves.
Mural Health is a participant management platform that helps manage & streamline the trial experience for patients and caregivers. Using modern payment, transportation, and communication solutions we help drive retention, compliance, and data quality.
Rho, a contract research organization (CRO) located in Chapel Hill, NC, provides a full range of services across the entire drug development process. For more than 30 years, Rho has been a trusted partner to leading pharmaceutical, biotechnology, and medical device companies as well as academic and government organizations. Our commitment to excellence, innovative technologies, and therapeutic expertise accelerate time to market, maximize returns on investment, and lead to an exceptional customer experience.
It was very interesting, both the presentations and the meeting opportunities.
IBSA Institut Biochimique SA
A great networking opportunity.
Medigene AG
See What It's All About
2025 Agenda
19 May 2026
20 May 2026
Expand All
Streams
Stream one
Clinical Operations and Outsourcing
Stream two
Clinical Technology and Innovation
12:45 PM
Innovations in patient recruitment, powered by AI
Understand how AI is revolutionizing how content is rated and qualified by enhancing precision and accelerating the speed of communication
Experience a real-life AI application used to optimize patient recruitment materials
Gain insights into future trends and opportunities in AI-powered translation for the life sciences sector, including regulatory compliance for labeling
Speakers
Stephane Millet
Director, Clinical and Patient Engagement Solutions, Acolad Life Sciences
Kathleen O’Brien
Head of Sales, Acolad Life Sciences
10:30 AM
Morning refreshments and networking break
Streams
Stream one
Clinical Technology and Innovation
9:45 AM
TECHNOLOGY SPOTLIGHT: Establishing data governance as a best practice in your clinical eco-system
Join for an insightful session on the world of data governance and security for the modern biotech. In this session, we will provide invaluable insights and practical strategies to help you optimize your clinical trial operations while ensuring the security of your sensitive data. Gain insight into areas such as mastering your data, the role of data governance in life sciences, and solving challenges in implementing data governance within your organization.
Speakers
Cat Hall
Head of GXP Assurance, Egnyte
Streams
Stream one
Clinical Operations and Outsourcing
Stream two
Clinical Technology and Innovation
11 AM
PANEL: Innovation and technology in clinical trials: exploring emerging and upcoming trends
• Is decentralization of clinical trials still relevant in 2025?
• Incorporating remote monitoring tools such as wearables into clinical trials
• An overview of new tools and solutions available on the market
• The growth of GenAI: when will this become widely used in clinical research?
• Balancing new techno
PANELLISTS:
Ashlyn Jose, Director, Clinical Operations, Kyowa Kirin, Inc
Ram Raju, Senior Vice President and Community Health Investment Officer, Northwell Health
Kristen Olszyk, Vice President, Clinical Operations, Neuraptive Therapeutics
Stefanie Kuhner, Head of Clinical Technology, Innovation and Patient Recruitment, Bristol Myers
Squibb
Speakers
Rich Polgar
Director Global Procurement, Bristol-Myers Squibb
Ashlyn Jose
Director, Clinical Operations, Kyowa Kirin, Inc
Ram Raju
Senior Vice President and Community Health Investment Officer, Northwell Health
Global Head Of Clinical Technology, Innovation & Patient Recruitment – Strategic Sourcing & Procurement, Bristol Myers Squibb
11:30 AM
Community is the new site: redefining trial footprints to expand access
As the clinical research industry pushes toward innovative solutions to increase inclusivity and access, it’s time to look beyond traditional site-based trial models and digital platforms. Expanding access isn’t just about technology-centered solutions – it’s about rethinking where and how trials happen. This session explores how community-based research models, including mobile research sites, mobile clinicians, and flexible visit options, are redefining what it means to bring research to patients. This session will explore how building trust and presence in local communities leads to better enrollment, stronger retention, and more representation data.
Speakers
Nancy Lizzul
Director, Site Operations, EmVenio Research
12 PM
CASE STUDY: Getting a new site up and running: challenges, opportunities and lessons learned
Top tips for working with and supporting naïve physicians in order to ensure their success
The importance of new study sites as a way of meeting FDA diversity requirements
Lessons learned for the future: what should you consider when working with naïve doctors?
Carrie Lewis, Executive Director, Clinical Program
Optimization, Endo
Suzy Montanye, Site Relationship Manager, Endo
Speakers
Carrie Lewis
Executive Director, Clinical Program Optimization, Endo Pharmaceuticals
Suzy Montanye
Site Relationship Manager, Endo Pharmaceuticals
12:30 PM
Achieving submission excellence with Certara’s regulatory operations solutions
Defining the full lifecycle of clinical and regulatory documents
Identifying practical actions authors can take to facilitate compliance with electronic regulatory submission requirements
Describing how technology tools are used to ensure efficient workflows and regulatory compliance
Speakers
Evan Richardson
Senior Director, Regulatory Operations and Clinical Disclosure, Certara
1 PM
Lunch and networking
2 PM
PANEL: AI and machine learning in clinical trials: where are we in 2025?
Opportunities for incorporating AI into clinical research: where should the industry be focusing?
Why has pharma been relatively slow to utilize AI in clinical research?
Understanding limitations of GenAI: what do you need to be wary of?
Real case studies on AI in the clinical trial industry: where has there been progress and success?
What does the future hold for AI in clinical trials?
MODERATOR:
Judyth Zahora, Senior Director, Clinical QA and Process Improvement, Zentalis Pharmaceuticals
PANELLISTS:
Rosanne Petros, Associate Director, Clinical Research, Merck Research Laboratories
Bryan Clayton, Clinical Systems Consultant, Alnylam Pharmaceuticals
Paresh Patel, Head of Global Clinical Intelligence, Otsuka
Speakers
Rosanne Petros
PMP, Associate Director, Clinical Research, Merck Research Laboratories
Bryan Clayton
Chief Commercial Officer, Endpoint Clinical
Paresh Patel
Head Of Global Clinical Intelligence, Otsuka
Judyth Zahora
Senior Director, Global Quality Systems and Process Improvement, Agenus
2:30 PM
Expanding the patient universe: transforming clinical trials through inclusive, data-driven design
Discover how integrating health equity & SDoH data improves patient representation and accessibility in clinical trials
Learn how H1 supports sponsors in designing inclusive, patient-centric trials to meet diversity action plan requirements and feasibility benchmarks
Explore real-world applications of inclusive research strategies that have successfully expanded patient diversity and engagement
Speakers
Chris Riley
Ph.D, Senior Product Manager, H1 Clinical
3 PM
Topic TBC
Dr Thomas Hopkins, Chief Medical Officer, AccuVein
3:30 PM
Afternoon refreshments, networking
4 PM
Health literacy in clinical trials: ensuring information is clear and accessible to patients
Technology and innovation for addressing health literacy and how information is presented to patients
Integrating health literacy principles into all phases of clinical research
How low health literacy can
Speakers
Lucas Goren
Senior Project Manager, CISCRP
4:30 PM
CASE STUDY: Practical aspects of running a clinical trial when repurposing an existing drug
Benefits of repurposing: how this can save time and money, and reduce risk to patients
How to effectively utilize real world data when repurposing existing drugs
Speeding up regulatory approval for a repurposed drug: how to navigate FDA guidelines
Speakers
John Seman
Chief Executive Officer, REVITALE Pharma
7:30 AM
Registration & Refreshments
8:30 AM
Chairperson’s opening remarks
Speakers
Rosalie Filling
Vice President, Senior Global Head R&D Operations, Endo Pharmaceuticals
8:45 AM
Evolving sourcing needs and models in clinical R&D
Clinical R&D outsourcing needs and models have evolved over the last few years. Many biopharma companies are transitioning to a function-driven sourcing model where we can have a set of fit-for-purpose preferred suppliers to bring in flexibility and agility. Challenges in sourcing needs, pros and cons of different sourcing models will be discussed.
Speakers
Mohan Bangalore
Senior Director, Procurement and Vendor Management, Summit Therapeutics
9:15 AM
Smarter, faster, autonomous: the future of clinical data management with generative and agentic AI
How Generative AI can streamline clinical data review, enhance efficiency, and reduce operational burden
Agentic AI’s potential to elevate data management from task-based automation to intelligent, autonomous systems
Real-world applications demonstrating the impact of AI-powered agents in clinical trial oversight
What’s next in AI evolution and how to prepare your data management processes for scalable change
Speakers
Prasanna Rao
Chief Products and Innovation Officer, Saama
9:45 AM
PANEL: Diversity in clinical trials: how to ensure your clinical study has diverse representation
Addressing historical issues with trial recruitment in certain populations in order to ensure diversity
Community outreach as a method to reduce distrust around clinical trial participation
Sourcing new sites in communities with high numbers of under-represented populations
Language and translation: how to ensure your trial materials are accessible to non English speaking participants
Speakers
Ram Raju
Senior Vice President and Community Health Investment Officer, Northwell Health
Patrick Floody
Executive Director, Global Clinical Trial Services
Innovative approaches to measure your performance and identify areas for improvement in supplier relationships
KPIs in clinical research: what should you be measuring to determine your performance?
Working collaboratively with your CROs and vendors throughout your clinical trial: where are you falling short?
Tools and technology available to facilitate processes around performance measurement
Speakers
Jim Mordaga
MBA, MA, Senior Director, Medical Platforms and Intelligence, Novartis
Amanda Murphy
Senior Director, Data Intelligence & Solutions, GlobalData
11:30 AM
Reserved for ICON Plc
12 PM
PANEL: Best practice in supplier relationship management: managing evolving needs to foster positive collaboration
• Priorities and considerations when working with vendors and external suppliers
• Cultivating collaborative relationships with vendors and CROs
• Managing procurement and outsourcing during an integration of two companies
• Developing a plan for effective supplier relationship management to ensure your trial runs smoothly
MODERATOR:
John Seman, Chief Executive Officer, Revitale Pharma
PANELLISTS:
Albert A Siha, Group Lead Director, Oncology, Internal Medicine, and Inflammation & Immunology, Pfizer Nupur Modi Murali, Director, Clinical Operations, Bausch Health Kathleen Cohen, Senior Vice President, Clinical Development Operations, Avalo Therapeutics Susan Neal, Senior Director, Clinical Operations, Novavax
Speakers
John Seman
Chief Executive Officer, REVITALE Pharma
Albert A Siha
Director, Oncology Unit Management Office, Procurement and Supplier Relationship Manager, Pfizer
Trump Administration effect on healthcare through the lens of a former regulator
Healthcare themes in a Trump Administration
Update on key priorities and opportunities
Short and long term effects of staffing and budget cuts
Speakers
Patrick Ronan
Operating Partner, ArchiMed and Board of Directors, Symbio Research
1 PM
Lunch and networking
2 PM
Marriage counseling: how two nurses from both the hospital and industry side see us resolving the site v sponsor chasm
What sites really want and need, and why they don’t understand sponsors
What sponsors really want and need, and why they don’t understand sites
Areas of common ground
How sites and sponsors can reconcile and work together to find success
Speakers
Linda Miller
Senior Clinical Operations Lead, Incyte
Todd Nicklas
Clinical Trial Manager, Incyte
2:30 PM
Built different: how a BioA-rooted central lab delivers precision in a dynamic clinical landscape
Most central labs are built to process samples. Ours was built to understand them. Evolving from a world-class bioanalytical backbone, Frontage Central Lab brings scientific depth, quality rigor, and operational discipline to every protocol, amendment, and shipment. This talk unpacks how our BioA heritage uniquely equips us to manage complex sample logistics, adapt to protocol deviations, and align with today's complex and evolving clinical trials!
Speakers
Dr Nan Zhang
Senior Vice President, Central Lab, Biomarker and Biologics Services, Frontage Laboratories
3 PM
PANEL: Handling clinical trial finances: tips for managing funding, investment and budgets
• Ensuring your trial is cost-conscious and efficient without compromising on quality or on patient care
• Forecasting and budgeting in order to accurately predict costs and minimize unforeseen expenses
• Keeping your clinical budget on track
• Negotiating prices and contracts in order to ensure maximum benefit without going over budget
Visit our exhibitors’ booths throughout the day and collect stamps in order to enter our Prize Draw and be in for a chance of winning Apple devices or Amazon gift cards. The Prize Draw will take place in the Exhibition Hall, make sure you don’t miss out!
4 PM
What does patient centricity mean in an outsourcing context?
Ensuring patients are at the forefront of conversations with CROs and vendors
Considering vendor selection processes with the patient in mind: what does this look like?
Working closely with patient advocacy groups alongside CROs and vendors to deliver a patientcentric clinical trial
Speakers
Amber Knight
Associate Director, R&D Procurement, Organon
4:30 PM
Reserved for Harvest Integrated Research Organization (HiRO)
5 PM
KEYNOTE PRESENTATION AND WORKSHOP: Applying AI to our clinical operations challenges
What’s stopping us from using AI?
How to overcome barriers to AI: creative starter ideas
AI case studies, stories and key takeaways
Speakers
Dan Seewald
Co-Founder and COO, LiviWell and Founder and CEO, Deliberate Innovation
5:45 PM
Chairperson’s closing remarks
Speakers
Rosalie Filling
Vice President, Senior Global Head R&D Operations, Endo Pharmaceuticals
5:50 PM
NETWORKING DRINKS RECEPTION AND END OF DAY 1
Streams
Stream one
Clinical Operations and Outsourcing
Stream two
Clinical Technology and Innovation
9 AM
Medically underserved populations and the impact on rare disease clinical trials
Insights on the differences between represented and underrepresents populations on their barriers to care
Challenges and nuances of rare disease patients’ journey to receive a diagnosis
Mental health and well-being: the emotional toll rare diseases take on patients and caregivers
Exploring overall experiences individuals have had within the healthcare system: strengths and areas for improvement
Harsha K. Rajasimha, MS, Ph.D, Founder and Executive Chairman, Indo US Organization for Rare Diseases
Speakers
Harsha K. Rajasimha
MS, Ph.D, Founder and Executive Chairman, Indo US Organization for Rare Diseases
9:30 AM
The innovation mandate: how to thrive in a rapidly evolving world of data and analytics
The current landscape of technology and analytics including some of the notable recent advances
How new technologies (eg GenAI and Predictive Modeling) can change the life sciences industry
What we need to do today to see tangible value and be ready to adapt to future developments
Speakers
Walter Boyle
Executive Director, Biostatistics and Programming
10 AM
A YEAR ON UPDATE: Critical to quality factors Part 2: operationalization of the concept in a pilot study
Jehan Poco, Associate Director, BDM Planning and Functional Excellence, Biostatistics and Data Management, Daiichi Sankyo, Inc
Kevin Douglass, Associate Director, RBQM Center of Excellence, Biostatistics and Data Management, Daiichi Sankyo, Inc
Speakers
Jehan Poco
Associate Director, BDM Planning and Functional Excellence, Biostatistics & Data Management, Daiichi Sankyo, Inc
Kevin Douglass
Associate Director, RBQM Center of Excellence, Global Clinical Operations, Daiichi Sankyo, Inc
10:30 AM
Morning Refreshments & Networking
11:15 AM
PANEL: Optimizing remote data capture: new trends and technology in data acquisition
Incorporating innovative products and tools into your clinical trial for remote data capture
FDA regulatory guidance around data acquisition and collecting data in remote settings
Easing burden on patients through remote data collection: how to utilize these tools effectively
How new tools such as eCOA solve patient issues
MODERATOR:
Terry Katz, Senior Director, Biostatistics and Data
Management Planning and Functional Excellence, Daiichi
Sankyo, Inc
PANELLISTS:
Robert Besthof, Chief Operating Officer, RiboNova
TJ Sharpe, Patient Advocate
Further panellists to be confirmed
Speakers
Terry Katz
Senior Director, Biostatistics, Data Management Planning, Functional Excellence, Daiichi Sankyo
Robert Besthof
Chief Operating Officer, RiboNova
11:45 AM
Leveraging technology for seamless collaboration
This session will include demonstrations and case study data illustrating how novel, effective technology-driven strategies can remove workflow friction and improve project delivery across several clinical workflows that are complex and dynamic, requiring multi-stakeholder inputs and timely, complex data exchanges. In this session, you will learn how to optimize your processes for patient eligibility review, remote monitoring and more – all in one collaboration platform!
Speakers
Jamie Russo
Head of Product, AG Mednet
8 AM
Registration and Refreshments
8:50 AM
Chairperson’s opening remarks
Speakers
Rosalie Filling
Vice President, Senior Global Head R&D Operations, Endo Pharmaceuticals
9 AM
PANEL: Ensuring your FSP model is a success: what do you need to know?
• Working closely with FSP vendors: how much oversight do you need?
• Benefits and challenges of moving to an FSP outsourcing model
• Comparing vendor management strategies between pharma and biotechs: do you need a different
approach?
• Why is FSP becoming a popular outsourcing model: what benefits can this offer sponsors?
PANELLISTS:
Melanie Goodwin, Director, Clinical Outsourcing,
Immunocore
Russell Bland, Director, Clinical Outsourcing and
Innovation, Jazz Pharmaceuticals
Terry Katz, Senior Director, Biostatistics and Data
Management Planning and Functional Excellence, Daiichi
Sankyo, Inc
Speakers
Rich Polgar
Director Global Procurement, Bristol-Myers Squibb
Melanie Goodwin
Director, Clinical Outsourcing, Immunocore
Russell Bland
Director, Clinical Outsourcing and Innovation, Jazz Pharmaceuticals
Terry Katz
Senior Director, Biostatistics, Data Management Planning, Functional Excellence, Daiichi Sankyo
9:30 AM
What do you mean you need equipment? Demystifying the complexities of the equipment supply chain
Explore the critical role of equipment in enabling clinical trial success, from ensuring compliance to supporting protocol-specific needs
Understand key challenges in the equipment supply chain, including global logistics, maintenance, and vendor management
Discover practical solutions such as centralized planning, global harmonization, and the use of technology to optimize supply chain performance
Learn from real-world examples that illustrate how proactive equipment management can save time, reduce costs, and ensure continuity across trials
Speakers
Jonathan Raven
Chief Commercial Officer, Emsere Bryan Dunlap, Business Development Manager, North America, Emsere
10 AM
PANEL: Preparing for an FDA inspection: common pitfalls and ensuring your study is ready for approval
Reviewing last year’s FDA feedback on audits: what were the main reasons for failure?
Tips and tricks to ensure you are ready for inspection
Simplifying processes in order to prepare for an FDA inspection
Speakers
Judyth Zahora
Senior Director, Global Quality Systems and Process Improvement, Agenus
Samantha Beddows
Director, Data Management, Oncology, AstraZeneca
10:30 AM
Morning refreshments and networking
11:15 AM
Choosing CRO and vendor partners as a small biotech sponsor: priorities and key considerations
• How vital is knowledge of therapeutic area in CRO selection?
• As a small biotech, is it beneficial to work with a smaller CRO or a large global CRO?
• Ensuring your CRO and vendor partners prioritize your study
11:45 AM
Driving success: strategies for optimal site support
Understand how the increasing complexity of clinical trials, higher competition, and site staff turnover are driving the need for more engaged site support
Learn how (CROs) provide crucial support through improved communication and tailored site resources
Explore how sponsors can enhance site performance through clear expectations and data-driven collaboration
Discover strategies for streamlining processes and improving site engagement to drive trial success
Speakers
Eleanor Miller
Clinical Trial Liaison, PSI CRO
12:15 PM
The state of the biopharmaceutical industry in 2025
Key themes and technology advancements in biopharma
Spotlight on clinical trial technologies for drug development
Leveraging data to predict the outlook for 2025 clinical trial outsourcing
Trends, key players, opportunities and threat in biopharma
What the latest investment trends show for small to medium biotechs
Speakers
Amanda Murphy
Senior Director, Data Intelligence & Solutions, GlobalData
12:45 PM
Lunch and Networking
1:45 PM
KEYNOTE PRESENTATION: Establishing a Center of Excellence for gene therapy and vaccines
Speakers
Gurdyal Kalsi
Chief Medical Officer, Asklepion Pharmaceuticals
2:15 PM
PANEL: Navigating the outsourcing landscape for emerging therapy areas
An overview of emerging therapy areas including women’s health, cell and gene therapy and rare diseases
Designing a successful patient recruitment strategy: common challenges and how to overcome these
Vendor sourcing: key considerations in vendor selection
How important is therapeutic area knowledge when choosing CROs and partners?
MODERATOR:
Judyth Zahora, Senior Director, Clinical QA and Process Improvement, Zentalis Pharmaceuticals PANELLISTS:
Gurdyal Kalsi, Chief Medical Officer, Asklepion Pharmaceuticals
Mohan Bangalore, PhD, Director, Global R&D Procurement and Supplier Management, Organon
Harsha K. Rajasimha, MS, Ph.D, Founder and Executive Chairman, Indo US Organization for Rare Diseases
Priya Marreddy, Vice President, Clinical Operations, OnCusp Therapeutics
Speakers
Judyth Zahora
Senior Director, Global Quality Systems and Process Improvement, Agenus
Gurdyal Kalsi
Chief Medical Officer, Asklepion Pharmaceuticals
Mohan Bangalore
Senior Director, Procurement and Vendor Management, Summit Therapeutics
Harsha K. Rajasimha
MS, Ph.D, Founder and Executive Chairman, Indo US Organization for Rare Diseases
Visit our exhibitors’ booths throughout the day and collect stamps in order to enter our Prize Draw and be in for a chance of winning Apple devices or Amazon gift cards. The Prize Draw will take place in the Exhibition Hall, make sure you don’t miss 0ut!
3:15 PM
PROBLEM-SOLVING ROUNDTABLE DISCUSSIONS
During the roundtable discussion session, the conference hall will be divided into four ‘zones’. Delegates can choose which zone they would like to join. Each zone will focus on a different challenge within clinical operations.
ROUNDTABLE 1: Developing a successful Diversity Action Plan for your clinical trial ROUNDTABLE 2: Creating an AI strategy to support clinical research ROUNDTABLE 3: Key considerations when selecting a CRO ROUNDTABLE 4: Working with advocacy groups to keep the patient voice at the heart of your trial
4:15 PM
End of conference
END OF CONFERENCE – SEE YOU NEXT YEAR!
2025 Speakers
Select a speaker to learn more
Back
Amber Knight
Associate Director, R&D Procurement, Organon
Session Details:
What does patient centricity mean in an outsourcing context?
2025-05-20, 4:00 PM
Session Details:
PANEL: Handling clinical trial finances: tips for managing funding, investment and budgets
Lauren joins us with over 25 years of pharmaceutical development experience in both large and small pharmaceutical company settings. Her career started as a clinical monitor with Covance which eventually led to oversight of clinical and medical affairs operations teams at Wyeth, Pfizer, Cephalon and Teva across multiple therapeutic areas. Her biotech experience includes Head of Clinical Operations and Project Management at Recro Pharmaceuticals and, more recently, Head of Clinical Operations at Aceragen Pharmaceuticals (formerly Idera Pharmaceuticals). She is currently Vice President of Clinical Operations at MapLight Therapeutics.
Lauren holds a BS in Biology from the University of Scranton and an MBA in Biotechology and Health Industry Management from Pennsylvania State University.
Session Details:
PANEL: Handling clinical trial finances: tips for managing funding, investment and budgets
John Seman is the CEO and Founder of REVITALE Pharma. He began his career working in Big Pharma - Johnson & Johnson and Bristol Myers Squibb - in sales, marketing and business development. The second half of his career was spent as a serial entrepreneur having Founded a half dozen companies that provided either products or services for the pharmaceutical industry. John earned his bachelor's and master's degrees from the Massachusetts College of Pharmacy.
Session Details:
PANEL: Best practice in supplier relationship management: managing evolving needs to foster positive collaboration
2025-05-20, 12:00 PM
Session Details:
CASE STUDY: Practical aspects of running a clinical trial when repurposing an existing drug
Kathleen Frenia Cohen is Vice President and Head of Clinical Development Operations at Marinus Pharmaceuticals. Prior to joining Marinus, she spent 20+ years at PRA Health Sciences in a variety of project management and operational oversite roles. Kathleen graduated from the University of the Science in Philadelphia with a PharmD and completed a post-doctoral fellowship in Pharmacoeconomics and Outcomes Research from Rutgers College of Pharmacy. Kathleen resides in Media, PA.
Session Details:
PANEL: Best practice in supplier relationship management: managing evolving needs to foster positive collaboration
2025-05-20, 12:00 PM
Session Details:
PANEL: Diversity in clinical trials: how to ensure your clinical study has diverse representation
Senior Director, Data Intelligence & Solutions, GlobalData
Amanda Murphy is the Director of Product Management at GlobalData, a company that focuses on research, data analytics and consulting that provide actionable insight into the pharmaceutical and medical device sectors. She has 10+ years of experience working in pharmaceutical data science and web platform development (including BioPharm Insight, Lead Sheet, and the Pharma Intelligence Center). She has developed models and solutions to support Clinical Operations & Feasibility teams plan and optimize trials, including an e-feasibility questionnaire tool resulting in 4x faster response rates from sites. Amanda also has many years of experience supporting business development at CROs through data-driven lead delivery and CRM integration solutions.
Session Details:
Innovative approaches to measure your performance and identify areas for improvement in supplier relationships
2025-05-20, 11:00 AM
Session Details:
The state of the biopharmaceutical industry in 2025
Senior Vice President and Community Health Investment Officer, Northwell Health
Dr. Ram Raju has a distinguished career over 40 years as a healthcare provider, teacher, researcher and community organizer. In his role at Northwell Health, Dr. Raju set the strategic vision to improve population health by finding ways to meet the needs of its most vulnerable communities, by examining the existing programs aimed at improving the health system's response to the community's needs and working with local organizations to address them. Northwell Health is the largest healthcare provider in the state of New York, is a system with 23 hospitals and 830 outpatient facilities that sees 2 million people every year in the New York metro area and beyond.
Session Details:
PANEL: Diversity in clinical trials: how to ensure your clinical study has diverse representation
2025-05-20, 9:45 AM
Session Details:
PANEL: Innovation and technology in clinical trials: exploring emerging and upcoming trends
Executive Director, Global Clinical Trial Services
Patrick has over 27 years’ experience in new drug development. He joined Regeneron in March 2020. His current role is the Head of the Global Clinical Trial Services group, responsible for global site management, central monitoring, study feasibility and site selection, study/site start up and eCOA and patient technology initiatives.
Prior to this, Patrick spent 25 years at Pfizer, with most of his time spent in clinical program operations but also includes GCP Quality (level 1) and Analytics. Patrick has extensive international experience in drug development. He helped establish the Pfizer country office development teams in Latin America, India and other parts of Asia. Subsequently, Patrick spent 10 years in Pfizer’s Development Japan organization as Head of Japan Development Operations and Development Japan Portfolio & Project Management Groups. He was the recipient of the PGRD Achievement Award in 2007.
Patrick is a former officer in the U.S. Army and is a veteran of the first Gulf War. He holds a bachelor’s degree in Biology from the University of Rhode Island and a Master of Business Administration from Temple University.
Session Details:
PANEL: Diversity in clinical trials: how to ensure your clinical study has diverse representation
Prasanna Rao is a distinguished AI practitioner and industry thought leader, currently serving as the Chief Products and Innovation Officer at Saama. With over 30 years of experience in information technology and analytics, including more than a decade in healthcare and life sciences, Prasanna brings a wealth of knowledge and expertise to his role.
Previously, as Global Head of AI/ML, Clinical Data Sciences at Pfizer Research & Development, Prasanna worked closely with stakeholders, vendors, business SMEs, machine learning developers, and data scientists to foster innovation and advance the adoption of AI in clinical data sciences. His tenure at IBM Watson as a Watson Solution Architect was marked by significant achievements in implementing AI systems for a diverse range of clients.
An accomplished speaker, Prasanna regularly presents at major industry conferences, including SCDM, DIA, SCOPE, DPharm, Tufts University CSDD, and Outsourcing Clinical Trials (OCT). He is also the holder of an IBM patent titled "Monitoring Clinical Research Performance," further cementing his status as a leading authority in leveraging technology for clinical development in the pharmaceutical industry. Prasanna continues to drive transformative advancements in AI and machine learning, delivering groundbreaking solutions to accelerate clinical research and development.
Session Details:
Smarter, faster, autonomous: the future of clinical data management with generative and agentic AI
Senior Director, Biostatistics, Data Management Planning, Functional Excellence, Daiichi Sankyo
Terry Katz is Senior Director of Biostatistics and Data Management Planning and Functional Excellence at Daiichi Sankyo. Previously he was Head of Global Data Management and Statistics at Merck Animal Health, Head of Biometrics at ImClone Systems, Senior Manager of Analysis & Reporting for PRA International, and a Statistician at Schering-Plough. He holds Accreditation as a Professional Statistician and Certifications as a Quality Engineer and a Six Sigma Green Belt. He is Chair of DIA's GCP-QA Community; formerly he was a Core Committee member for NJ CDISC User Group and Chair of the Statistical Taskforce for the Animal Health Institute. Terry also completed a 3-month Fellowship in Kenya to improve capacity and capability for the local hospitals to run oncology clinical trials.
Session Details:
PANEL: Ensuring your FSP model is a success: what do you need to know?
2025-05-21, 9:00 AM
Session Details:
PANEL: Optimizing remote data capture: new trends and technology in data acquisition
Vice President, Senior Global Head R&D Operations, Endo Pharmaceuticals
In her over 25 years of experience, Rosalie “Rosie” Filling has transformed R&D operations in every company she has worked for, developing clear-cut strategies to help advance clinical trials with high-quality operational execution and scientific excellence.
Rosie is the Vice President, Senior Global Head R&D Operations Endo International plc. She is part of the global R&D leadership team and is charged with the coordination and implementation of clinical development strategies for the company’s research and development. She provides strategic direction and oversight of the R&D Operations team, which includes clinical operations, data management, biostatistics, medical writing, clinical supplies, trial master file/inspection readiness and business operations. This integrated team handles the execution of all aspects related to Endo’s clinical trials. Endo has active research and development programs in men’s health, orthopedics, and endocrinology. Beyond these therapeutic areas, the company also has focused development in the areas of sterile injectables and complex generic products.
Rosie’s main focus at all times is on the end users—the patients. Bringing new and, at times, life-saving medications to patients drives Rosie’s sense of purpose.
Rosie joined Endo from Lupin Pharmaceuticals in Blue Bell, PA where she was Senior Director, Head of Clinical Operations, and built the clinical operations organization to support the US and Global R&D Organization. Prior to Lupin, Rosie spent nearly five years at Teva in Frazer, PA where she was the US site head of Clinical Operations and was responsible for the successful delivery of Inhalation, Women’s Health, and Cardiovascular clinical trials. Earlier in her career, Rosie held various roles at Eisai, MGI Pharma and PPD.
Rosie earned her B.S. in Biology with a minor in Chemistry from the University of Pittsburgh.
Kristen Olszyk joined Neuraptive in March 2020 and is the Acting Head of Clinical Operations. She brings with her 20 years in the pharmaceutical industry. Kristen’s areas of expertise include data science, clinical development, clinical operations and regulatory affairs, and she has been involved with several successful regulatory submissions in multiple therapeutic areas. Prior to joining Neuraptive, Kristen held positions at Wyeth Pharmaceuticals/Pfizer, Endo Pharmaceuticals and Paratek Pharmaceuticals.
Kristen earned her Bachelor of Science degree in Biochemistry from The Pennsylvania State University and her Master of Science degree in Quality Assurance and Regulatory Affairs from Temple University School of Pharmacy.
Session Details:
PANEL: Innovation and technology in clinical trials: exploring emerging and upcoming trends
PMP, Associate Director, Clinical Research, Merck Research Laboratories
Rosanne Petros is a US Sr. Clinical Research Manager currently working in the vaccine therapy area. She has 35 years of experience in Clinical Research primarily in clinical project management and is a PMP. She has been at Merck for 18 years. Prior to Merck, Rosanne had her own clinical research consulting company and began her career in clinical research at Pharmaco (then PPD). Rosanne received her degree in Chemistry from University of Virginia and was a bench chemist prior to moving into clinical research. She lives outside of Washington DC with Kevin, her husband of 35 years and 4 of her 5 children (one moved out!) and two shih tzu mix dogs. Her children range in age from 30 to 13 years old. Rosanne enjoys cooking, crafting and being with her family. She also enjoys collecting and restoring Victorian and Art Deco jewelry and collecting and repairing vintage quilts.
Session Details:
PANEL: AI and machine learning in clinical trials: where are we in 2025?
Bryan Clayton is a seasoned global commercial leader with experience across multiple functions including sales and marketing, operations, and software product design. For over 20 years, he has effectively managed cross-functional teams, created new technology solutions, managed contract negotiations, and driven revenue growth for top life sciences technology and solutions providers. Bryan is a sought-after speaker, writer and contributor to industry events and publications, and possesses a range of skills well-suited to boost commercial success and revenue growth.
Bryan joined endpoint Clinical in 2023 as Chief Commercial Officer to lead commercial strategy and business development operations, and to further strengthen endpoint’s expertise in providing agile, patient centric IRT solutions. In his spare time, Bryan coaching and playing baseball.
Session Details:
PANEL: AI and machine learning in clinical trials: where are we in 2025?
Executive Director, Clinical Program Optimization, Endo Pharmaceuticals
Carrie Lewis has over 20 years of varied Clinical Research experience. Carrie is currently an Executive Director, Clinical Program Optimization at Endo USA, Inc. where she oversees Clinical as well Business Operations, eTMF/inspectional readiness, and Training/Oversight. Prior to Endo, Carrie garnered extensive knowledge in many roles while in academia, at large sponsors, generic sponsor, as well as a global CRO. She has a Master’s Degree in Clinical Research Administration and has experience in multiple therapeutic areas.
Session Details:
CASE STUDY: Getting a new site up and running: challenges, opportunities and lessons learned
Chief Commercial Officer, Emsere Bryan Dunlap, Business Development Manager, North America, Emsere
Jon is a seasoned professional with over 20 years of experience and has demonstrated expertise in helping Pharma, Biotech and CROs solve complex and challenging development issues; ensuring clinical studies remain on their critical path to success. Throughout his tenured career, Jon has held pivotal roles at Pfizer and Avantor where he has made significant contributions to the development and launch of life saving and life changing medicines and he now brings that expertise to Emsere. As a speaker, Jon engages audiences with insightful discussions, drawing from his extensive experience and unique perspectives.
Session Details:
What do you mean you need equipment? Demystifying the complexities of the equipment supply chain
Eleanor Miller, Clinical Trial Liaison, is an oncology certified nurse with 17 years of oncology nursing experience at academic medical centers, including both inpatient and outpatient care, most recently leading an oncology nurse navigation program. Much of her career has been in direct collaboration with investigators and research teams to improve patient access to trials through increased awareness, patient education, and coordination of care.
At PSI, she uses this operational and clinical expertise to develop site specific recruitment strategies, tailored study tools and training. She can anticipate barriers to enrollment and resolve site needs with the project team. Eleanor is a strong collaborator and strategic thinker by identifying patterns, and bridging gaps between sites, clinical operations, project management, and sponsors.
Session Details:
Driving success: strategies for optimal site support
Associate Director, BDM Planning and Functional Excellence, Biostatistics & Data Management, Daiichi Sankyo, Inc
Jehan, Associate Director, Functional Excellence, Biostatistics & Data Management (BDM), Daiichi Sankyo, Inc.
Jehan is an Associate Director in the Biostatistics & Data Management Functional Excellence at Daiichi-Sankyo. In this role, Jehan partners with BDM and R&D teams on functional initiatives, system roll outs, and committee as well as supporting key partners like the RBQM COE as a member.
Jehan has 18+ years of industry experience working for numerous companies in various positions (TMF, Clinical Monitoring, Quality & Compliance, Operational Excellence/Change Management, Metrics/Benchmarking and RBQM). He received a BA in Cell Biology & Neuroscience from Rutgers College, an MBS in Biomedical Science from the University of Medicine and Dentistry NJ (UMDNJ), and is certified Auditing and Change Management methodologies.
Associate Director, RBQM Center of Excellence, Global Clinical Operations, Daiichi Sankyo, Inc
Kevin Douglass, Associate Director, RBQM Center of Excellence, Biostatistics & Data Management (BDM), Daiichi Sankyo, Inc.
Kevin is an Associate Director in the Risk-Based Quality Management Center of Excellence (RBQM COE) at Daiichi-Sankyo. The RBQM COE partners within BDM, with cross-functional stakeholders, and CRO partners to optimize RBQM processes and tools. The RBQM COE has central (e.g., as process owners developing and delivering tools and training) and Program/Study-level responsibilities (providing guidance to study teams).
Kevin has 40+ years of industry experience working for numerous companies in various positions (Data Management, Quality & Compliance, Operational Excellence/Change Management, and RBQM). He received a BS in Biology from Ursinus College, an MS in Biology from Villanova University, and is certified in Lean Six Sigma and multiple Change Management methodologies.
A 15-year veteran of the translation industry with a background in linguistics, Kathleen has held various roles in the translation business: vendor, project and account management, as well as new business development. Her experiences have positioned her with a unique perspective into both translation operations and how translation impacts the globalization needs of clients in the pharmaceutical and medical device industries. Kathleen proactively collaborates with her Life Sciences client partners on a daily basis to help them set their localization strategies.
Vice President, Senior Global Head R&D Operations, Endo Pharmaceuticals
In her over 25 years of experience, Rosalie “Rosie” Filling has transformed R&D operations in every company she has worked for, developing clear-cut strategies to help advance clinical trials with high-quality operational execution and scientific excellence.
Rosie is the Vice President, Senior Global Head R&D Operations Endo International plc. She is part of the global R&D leadership team and is charged with the coordination and implementation of clinical development strategies for the company’s research and development. She provides strategic direction and oversight of the R&D Operations team, which includes clinical operations, data management, biostatistics, medical writing, clinical supplies, trial master file/inspection readiness and business operations. This integrated team handles the execution of all aspects related to Endo’s clinical trials. Endo has active research and development programs in men’s health, orthopedics, and endocrinology. Beyond these therapeutic areas, the company also has focused development in the areas of sterile injectables and complex generic products.
Rosie’s main focus at all times is on the end users—the patients. Bringing new and, at times, life-saving medications to patients drives Rosie’s sense of purpose.
Rosie joined Endo from Lupin Pharmaceuticals in Blue Bell, PA where she was Senior Director, Head of Clinical Operations, and built the clinical operations organization to support the US and Global R&D Organization. Prior to Lupin, Rosie spent nearly five years at Teva in Frazer, PA where she was the US site head of Clinical Operations and was responsible for the successful delivery of Inhalation, Women’s Health, and Cardiovascular clinical trials. Earlier in her career, Rosie held various roles at Eisai, MGI Pharma and PPD.
Rosie earned her B.S. in Biology with a minor in Chemistry from the University of Pittsburgh.
Kathleen Frenia Cohen is Vice President and Head of Clinical Development Operations at Marinus Pharmaceuticals. Prior to joining Marinus, she spent 20+ years at PRA Health Sciences in a variety of project management and operational oversite roles. Kathleen graduated from the University of the Science in Philadelphia with a PharmD and completed a post-doctoral fellowship in Pharmacoeconomics and Outcomes Research from Rutgers College of Pharmacy. Kathleen resides in Media, PA.
Session Details:
PANEL: Best practice in supplier relationship management: managing evolving needs to foster positive collaboration
2025-05-20, 12:00 PM
Session Details:
PANEL: Diversity in clinical trials: how to ensure your clinical study has diverse representation
Vice President Of Clinical Development, Trefoil Therapeutics, Inc
Thomas is a registered nurse with both clinical and over 30 years pharmaceutical development experience. His pharmaceutical development experience includes clinical operations, clinical science, clinical development, drug safety and quality. He is currently Vice President of Clinical Development at Trefoil Therapeutics and adjunct faculty at San Francisco State University.
Next
Back
Behtash Bahador
Director, Health Literacy, CISCRP
Behtash Bahador is the Director of Health Literacy at the non-profit organization CISCRP, and holds a Master of Science in Health Communication from the Tufts University School of Medicine. Since 2014, he has collaborated with a range of stakeholder groups to establish and implement patient- and public-centric initiatives across the life-cycle of drug and treatment development. This has included supporting the development of regulatory and cross-disciplinary best practice guidelines, operationalizing key elements of evidence-based public health programing into research engagement activities, and always keeping the needs of patients, participants and the public at the forefront of his work.
Next
Back
Bao Dinh
Global Development Business Operation, Takeda
With over 15 years of experience in Clinical Data Management, Bao leads business strategy and vendor operations for Takeda’s Clinical Data Management, Clinical Data Engineering, and Clinical Data Standards groups, driving organizational growth, managing global FSP partnerships, and enhancing cross-functional collaboration. As a member of the 2024–2025 OCT Advisory Board, Bao brings expertise in clinical outsourcing, strategic vendor partnerships, and RFP process optimization, providing a fresh vision for the organization.
Beyond professional achievements, Bao is dedicated to fostering collaboration and investing in the local community. As a partner of The Town FC and a Silicon Valley angel investor, Bao champions ventures that advance sustainable growth, youth enrichment, and innovation in technology.’
Next
Plan Your Visit
Venue
Valley Forge Casino Resort
1160 1st Ave, King of Prussia, PA 19406, United States
Arena International Events Group “(Arena”) is aware of numerous third-party agencies which are contacting Arena’s customers and purporting to have access to hotel room bookings, events attendee lists and selling unsolicited services. It is unclear whether the agencies in question are in possession of such information, or whether they intend to scam unsuspecting customers. Whilst Arena International Events Group pursues such third-party companies for their potentially illicit activity, Arena encourages you to be cautious in engaging with such third-party agencies and Arena shall not accept any responsibility for any losses incurred by you should you choose to engage with third parties that have no affiliation to Arena International Events Group..
Sponsors
Select a sponsor to learn more
Featured Sponsor
Back
Company Information
Saama Technologies is the advanced clinical data and analytics company, unleashing wisdom from data to deliver better actionable business outcomes for the life sciences industry. Saama’s unified, AI-driven clinical data analytics cloud platform seamlessly integrates, curates, and animates unlimited sources of structured, unstructured, and real-world data to deliver actionable insights across all therapeutic areas. The award-winning platform gives unprecedented real-time visibility into clinical data, enabling sponsors to file New Drug Applications (NDAs) more efficiently to bring drugs to market faster and at lower costs. For more information, visit http://www.saama.com.
Company Website
To learn more, please visit our website -
www.saama.com
Session Sponsors
Back
Company Information
Certara accelerates medicines using proprietary biosimulation software, technology and services to transform traditional drug discovery and development. Its clients include more than 2,300 biopharmaceutical companies, academic institutions and regulatory agencies across 70 countries.
Back
Company Information
Cytel Inc.www.cytel.com is a leading provider of clinical research services and trial design and analysis software primarily for the biopharmaceutical and medical device development markets.
Cytel pioneered the statistical and computational science of adaptive clinical trials and has designed more validated adaptive trials than any other service provider.
Emsere is a medical equipment solutions provider dedicated to clinical trials and delivers full, global services to suit study-specific needs from their operational facilities in EU, USA and Singapore. Emsere leverages over 25 years of clinical trial experience to provide customers a worry-free clinical trial equipment experience. Just “Emsere it”.
Back
Company Information
Frontage is a CRO providing integrated, scientifically-driven research, analytical and product development services throughout the drug discovery and development process to enable biopharmaceutical companies to achieve their drug development goals. We are focused on helping our client’s to address their most significant and complex drug discovery and development challenges. Our scientific knowledge base, technical expertise and reputation for high quality services have been integral to our ability to turn our services into your solutions.
H1 harnesses and democratizes access to hard-to-assemble HCP information, claims data, ground-breaking research, and expert opinions. H1’s ability to gather and make sense of billions of data points and deliver them in workflow-friendly solutions helps to accelerate the development, launch, and dissemination of life-saving treatments; drive meaningful engagements with key opinion leaders; and help ensure equitable access to healthcare services.
Harvest Integrated Research Organization (HiRO) is an innovative CRO with global footprints in the US, Mainland China/Taiwan, Australia/New Zealand, South Korea, Malaysia, and the Philippines.
With global operations and integrated capabilities, HiRO provides a full range of cross-border solutions. We strive to work collaboratively with biotechs to bring new products from the laboratory to market.
ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organisations. We develop new innovations, drive emerging therapies forward and improve patient lives. With headquarters in Dublin, Ireland, ICON employed approximately 41,150 employees in 113 locations in 53 countries as at September 30, 2022.
PCM Trials has been at the forefront of decentralized clinical research since 2008, leading mobile visits and recently introducing community-based research sites. We are driving the shift to patient-centric clinical trials, giving individuals the flexibility to engage in research studies in ways that work best for them. Our approach expands opportunities for participation, resulting in greater patient diversity, reduced patient dropout, and faster study results.
PSI is a privately-owned, full-service contract research organization (CRO), operating globally. PSI’s reputation on the market place is that of a no-nonsense CRO, capable of saving pharmaceutical sponsors millions of development dollars by consistently meeting clinical trial timelines. PSI’s global reach supports the operations of clinical trials across multiple countries.
Symbio is a global full-service Clinical Research Organization (CRO) with a strong focus on Dermatology, Aesthetics and Inflammatory diseases. Managing all CRO core services in-house with offices in the USA and Europe. Delivering excellent service and providing experienced qualified personnel to strategically manage all aspects of your clinical trials. Symbio offers expertise in Proof-of-Concept, Medical Device and Phase 1 – Phase 4 clinical studies and has completed over 650+ clinical studies to date.
AG Mednet is revolutionizing the clinical trial process through Judi, the innovative and award-winning clinical trial collaboration platform. Designed to empower the ecosystems that drive clinical research, the proven platform Judi streamlines workflows, facilitates communication, and accelerates the development of novel therapies for patients. Judi is trusted by 19 of the top 20 global biopharmaceutical sponsors and 5 of the top 6 global CROs and enables clinical teams around the world to come together to seamlessly manage complex workflows in endpoint adjudication, central eligibility determination, data safety monitoring, medical imaging, remote monitoring, and other mission-critical areas of clinical development.
360biolabs is Australia’s most comprehensive bioanalytical laboratory providing support for development of new therapeutics, vaccines and diagnostics. We support pharmacokinetic (PK) analysis, pharmacodynamic (PD) endpoints in a quality assured environment (GLP, GCP, ISO / IEC 17025). We provide the advantage of a Phase 1 solution in Australia and transfer or continuation of your clinical study with our team in the USA or Europe.
The benefits of conducting early phase clinical trials in Australia:
Speed: No IND required, healthy volunteer study approval in ~4-6 weeks
Quality: Data recognized by global regulatory bodies (e.g. FDA, EMA)
ACM Global Laboratories is one of the largest global independent central labs in the industry. ACM is certified by the College of American Pathologists (CAP) and the Substance Abuse and Mental Health Services Administration (SAMHSA). The company delivers high-quality laboratory testing and diagnostic lab services in support of both clinical trials research, toxicology and individual patient care. ACM provides a powerful combination of operational excellence, scientific expertise and unsurpassed global service to customers in more than 65 countries. ACM performs more than 20 million laboratory tests each year—spanning all medical disciplines including pathology, microbiology, molecular diagnostics, toxicology and more.
Advanced Clinical is a global clinical research services organization, providing CRO, FSP, Strategic Resourcing and Consulting Services for biopharmaceutical and medical device organizations. Our company is committed to improving all lives touched by clinical research and we address the hopes of patients and healthcare professionals with industry-leading services and technology in life sciences. Visit our website to learn more about how we deliver a Better Clinical Experience.
The Almac Group is an established contract development and manufacturing organisation providing an extensive range of integrated services across the drug development lifecycle to the pharmaceutical and biotech sectors globally.
Its innovative services range from R&D, biomarker discovery development and commercialisation, API manufacture, formulation development, clinical trial supply, IRT (IVRS/IWRS) through to commercial-scale manufacture.
The international company is a privately owned organisation which has grown organically over the past five decades now employing over 5,600 highly skilled personnel across 18 facilities including Europe, the US and Asia.
The company has a global reputation for excellence built over 50 years of client service, delivering expertise right across the drug development lifecycle and offering a tailored solution to each of our clients.
To keep up to date with latest news, follow Almac Group on Twitter and LinkedIn or visit almacgroup.com.
Array is a trusted partner for pharmaceutical companies seeking to enhance their Investigator Meetings. With nearly two decades of experience and a track record of over 10,000 events, we specialize in delivering tailored solutions designed to drive impactful outcomes. Our innovative technology and services are meticulously crafted to engage participants effectively, ensuring over 90% audience engagement while facilitating seamless knowledge transfer and actionable insights. Array’s dedicated support team offers comprehensive service, from event execution to detailed analytics interpretation, empowering pharmaceutical companies to optimize the success of their in-person, virtual, and hybrid Investigator Meetings.
To learn more, please visit our website -
atreo.io
Back
Back
Company Information
With over 40 years’ experience, 600 beds and locations in NA, EU and Asia, Celerion conducts First-in-Human, clinical Proof-of-Concept and patient dose response studies, cardiovascular safety and NDA-enabling clinical pharmacology research. Celerion provides full study services including statistics, data management and biostatistics (including PK/PD analysis), and bioanalytical services.
Clario is a leading provider of endpoint data solutions that generate high-quality clinical evidence for our pharmaceutical, biotech, and medical device partners. We offer comprehensive evidence generation solutions that combine eCOA, cardiac solutions, medical imaging, precision motion, and respiratory endpoints. Since our founding more than 50 years ago, Clario has delivered deep scientific expertise and broad endpoint technologies to help transform lives around the world. Our endpoint data solutions have supported clinical trials over 26,000 times in more than 100 countries. Our global team of science, technology, and operational experts have supported over 60% of all FDA drug approvals since 2012.
Company Website
To learn more, please visit our website -
www.Clario.com
Back
Company Information
An agile CRO providing services for Phase 2 to 4 clinical trials in both Full-service and Functional Service Provider models. We have nearly a decade of experience in global trials across Neurology, Psychiatry, Oncology, Cardiovascular, and Gastroenterology, including Rare Diseases and Pediatric trials. Our proven expertise includes guiding an emerging biopharma through the complexities of bringing a new drug to market.
We are part of the $4 Billion J.K Group, a diversified, multinational conglomerate!
Comac Medical is focused on providing innovative and flexible solutions of the highest quality to meet pharmaceutical industry needs. Founded in 1997, we are CRO and SMO managing the full spectrum of clinical trial services from Phase I – IV across 30 European countries, the US and APAC. With applying our innovative solutions, we can ensure that the Clients’ projects are managed with the highest level of efficiency.
In 2005 Comac Medical started its state-of-the-art Clinical Research Unit for Phase I, BA/BE studies with 42 hospital beds, a highly qualified medical and operational team, a large patient/healthy volunteers database, an extensive referral physician network, and central laboratory/pharmacy services.
The company has a global reputation for excellence built over 25 years of offering tailored solutions to our Clients. To keep up to date with the latest news, follow Comac Medical on LinkedIn or
Danforth Advisors is the life science industry’s trusted partner for strategic and operational support across business, clinical, and commercial functions. The company advises and executes in the areas of finance and accounting, strategic communications, human resources, risk management, clinical and regulatory, market research, and commercial readiness and launch. Founded in 2011, Danforth has partnered with more than 1,500 life science companies, private and public, across all stages of the corporate lifecycle.
Deep 6 AI is the leader in precision research software, connecting all research stakeholders in an AI-powered, real-time, data-driven, collaborative ecosystem. Our Precision Matching software mines millions of patient records, including “unstructured” physician notes, to pin-point eligible study patients in real-time. Deep 6 eliminates months of manual data validation, to de-risk and accelerate clinical trials, because clinical trials should be a gatekeeper (accelerator), not a bottleneck to innovation.
Company Website
To learn more, please visit our website -
deep6.ai
Back
Company Information
eClinical Solutions is a leading global provider of cloud-based enterprise software and software-driven clinical data services. The elluminate® Clinical Data Cloud provides life sciences companies with greater control of their clinical trial data with one platform for all data sources, from aggregation through to standardization, visualization, and preparation for submission. elluminate software and data driven services have been used by more than 100 life sciences companies on over 500 clinical trials to reduce cycle time and improve data quality. For more information, visit www.eclinicalsol.com, or contact us at info@clinicalsol.com.
Egnyte combines the power of cloud content management, data security, and AI into one intelligent content platform. More than 22,000 customers trust Egnyte to improve employee productivity, automate business processes, and safeguard critical data, in addition to offering specialized content intelligence and automation solutions across industries, including architecture, engineering, and construction (AEC), life sciences, and financial services.
Endpoint Clinical is a leading clinical trial technology and service partner, delivering adaptable RTSM solutions with a focus on security, stability, and trust. With decades of expertise and a proactive, innovation-driven approach, Endpoint minimizes friction, reduces risk, and enables your teams to focus where it matters most—on trial success.
Complex innovative clinical trial designs require an integrated synergetic approach to assess novel drug compounds for safety and effectiveness which often span esoteric, regulated and safety outcomes in all phases of the drug development life-cycle.
The companies of Eurofins BioPharma Services provide a seamless solutions-based approach in support of phase I to IV clinical trials with a unique analytical testing portfolio for Central Laboratory Services, Bioanalytical Services and complex Biomarker Assay Development and Testing Services for drug and vaccine development.
Euromed Pharma deliver strategic services tailored to support companies in their quest to better healthcare. We support each industry player from drug development through the post-marketing phases. We offer solutions in CTS services, Clinical GMP Packaging, Labeling and Distribution, IMP management, Early Access and Named Patient Programs, Pharma Order to cash solutions, and Supply Chain & Logistics. We are present around the world with offices in Italy, Spain, Ireland, Germany, Singapore and the USA. Being one of the Petrone Group companies, Euromed Pharma is positioned at the forefront of innovation in pharmaceutical distribution.
Faro helps teams develop better clinical protocols that are more patient and site centric by connecting all the stakeholders in the clinical trials ecosystem through a single software platform. The Faro platform provides a best-in-class standardized library of clinical study activities with performance-related metadata to provide real-time actionable insights during protocol development. Faro brings transparency, trust, and predictability to protocol development.
Greenphire is the industry leader of clinical payment technology, designed to improve the way research professionals work. We leverage our proprietary payments platform and workflow automation to help clients improve operational efficiency, reduce costs, mitigate regulatory risks, improve the patient and site experience and produce quantifiable results that improve clinical operations and strategic planning.
Harbor Clinical, a WBENC-certified, women-owned company, provides a hybrid of services which ensure all aspects of clinical trials meet quality assurance and regulatory standards – from study documentation, vendor oversight, and flexible resourcing throughout operations. Developing and supporting your quality initiatives from Day 1, the Harbor team is committed to quality through each functional service we provide.
Imperial Clinical Research Services provides cost-conscious ancillary trial supplies and equipment procurement/management, premium print and digital production, award-winning creative design and writing of clinical trial materials, translation services for 100+ languages, targeted patient engagement programs, warehousing, and global logistics to more than 100 countries.
Infuserve America’s purpose is to partner with the clinical trial community to provide the highest quality central pharmacy services. A leader in the clinical trial industry, Infuserve America is experienced in many aspects of the decentralized clinical trial work including Direct to Patient and Direct to Site. Infuserve America is ready and able to partner with CROs, Pharmaceutical Companies, Sponsors, or individual sites to assist with IP dispense and distribution.
Founded in 2005, Inspire connects life sciences organizations with the voices that matter most—patients and caregivers. With 10 million unique annual visitors across over 3,000 disease states, Inspire leverages its engaged patient communities to accelerate clinical trial recruitment, uncover real-world evidence, deliver actionable market research, and provide targeted advertising solutions for health-focused audiences. By bridging the gap between patients and life sciences, Inspire enables smarter decision-making and a deeper understanding of the communities it serves.
Kayentis, a global leader in eCOA and Decentralised Clinical Trial solutions, empowers pharma, biotech, and CROs to streamline data collection in clinical trials, enhancing simplicity, efficiency, and data quality. Since 2005, Kayentis has spearheaded clinical development, specializing in eCOA solutions acros phases I-IV in diverse therapeutic areas. Adapting to the changing landscape, Kayentis now offers a comprehensive suite of services to support the shift towards decentralized and hybrid trials, with operational capabilities acros the USA, Europe and Asia.
Korio is the industry’s first compliance-centric Randomization & Trial Supply Management (RTSM) platform. Reflecting decades of hands-on experience across thousands of trial designs, Korio enables once aspirational goals around feature reusability, process repeatability, system performance, and overall system quality by embedding the latest RTSM design intelligence into our solution.
LabConnect is the world’s most agile central laboratory solutions partner supporting clinical trials of all sizes and complexity. With modern operations and strategic alliances with world-leading laboratories, LabConnect is uniquely positioned to provide access to the latest innovation and automation. LabConnect is the trusted partner for biotechnology, pharmaceutical, and clinical research organizations.
Our mission is to optimize the “Clinical Trial Ecosystem,” applying industry experience and the latest technology to streamline, secure, and enhance the interactions between sponsors, sites, CROs, and others involved in administering and operating clinical trials. Driven by a unique combination of deep domain expertise and technical capabilities, our ClinRun application suite rethinks trial administration through active engagement, smart design, and breakthrough technology. Enhance site negotiations and pay with ease, with the industry’s first Procure-to-Pay solution designed specifically for clinical trials.
MaxisIT delivers agentic AI-driven clinical trial data analytics, empowering life sciences teams with faster, smarter insights. With 3,300+ trials in cloud, our source-agnostic platform serves as a single source of truth. Backed by 20+ years of domain expertise, we simplify data management, accelerate timelines, and optimize outcomes across global clinical operations.
mdgroup supports all sizes of pharma and biotech to attract, engage, and maintain patient participation in healthcare research. With a pioneering global ecosystem of clinical trial solutions, streamlined patient reimbursements, safe patient transport and in-home health visits – to personalised patient support, clinical equipment logistics and top-tier healthcare professional staffing placements.
MedNet is a leading eClinical technology company specializing in electronic data capture and clinical study management systems. Since 2001, MedNet’s proven cloud-based solutions have successfully supported research initiatives worldwide. Visit our booth to see iMedNet eClinical…an agile, efficient and, effective solution that allows sponsors and CROs to easily build studies.
Metronomia is a German clinical research organization (CRO) committed to high quality, best service and outstanding flexibility. A service oriented, stable and highly skilled team provides e-clinical services,clinicaldata management and biostatistical services within phase I – IV and non-interventional studies in allmajor therapeutic areas.
Miller Tanner Associates is a WBENC-certified, full-service global corporate event planning company specializing in the life sciences industry for 26+ years (15+ in virtual events). We deliver exceptional experiences for face-to-face, virtual, and hybrid meetings and events as well as tailored event management technology solutions including proprietary tools – EPIC™, Attend™, and VALTs™. We offer a broad spectrum of products and services to support event planning needs, including security and compliance (21CFR Part 11), engagement strategies, technology support, robust pre- and post-event reporting, and more. To learn more about Miller Tanner Associates, visit https://www.millertanner.com/
MMS Holdings (MMS) is an award-winning, data-focused clinical research organization (CRO) that supports the pharmaceutical and biotech industries with a proven, scientific approach to complex trial data and regulatory submission challenges. Strong industry experience, a 19-year track record, AI technology-enabled services, and a data-driven approach to drug development make MMS a valuable CRO partner. With a global footprint across four continents, MMS maintains an industry-leading customer satisfaction rating. For more information, visit www.mmsholdings.com
Mural Health is a participant management platform that helps manage & streamline the trial experience for patients and caregivers. Using modern payment, transportation, and communication solutions we help drive retention, compliance, and data quality.
Myonex provides tailored services and solutions to advance medicine through clinical to commercial stages with tailored drug sourcing and ancillary supply, to packaging, labeling, and distribution. With ten global locations, we offer flexible, efficient, and cost-effective support for clients across the pharmaceutical and biotech sectors.
Company Website
To learn more, please visit our website -
www.myonex.com
Back
Company Information
We deliver comprehensive solutions across the therapeutic development lifecycle to unlock insights, accelerate research, advance therapeutics,
and integrate evidence into everyday care. By uniting cloud, data, AI, and decades of life sciences research expertise, we develop intelligent
solutions to bring safer, more effective therapies to market faster and more efficiently. Bridging life sciences and healthcare, we’re building
a learning ecosystem that accelerates innovation, personalizes treatments, speeds therapeutic development, and shapes the future of healthcare.
Oximio optimizes clinical trial supply chains, with consolidated logistics, clinical supply and patient-centric services. Our unique geographic footprint provides access to patient communities of 500m+ people though an owned operational depot network, and strategically located partners, within Europe, Middle East and Africa.
To learn more, please visit our website -
www.oximio.com
Back
Company Information
Prevail InfoWorks improves the probability of clinical trial success by providing stakeholders real-time actionable intelligence to effectively manage endpoints and key deliverables with the Single Interface™, its patented cloud-based tool that aggregates, reconciles, analyzes and single-view reports/visualizes all clinical, operational and project accounting data, regardless of the source or format.
For the past 20 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance scientific breakthroughs and introduce new therapies. As the world’s largest RCO (Research Consulting Organization), ProPharma partners with its clients through an advise-build-operate model across the complete product lifecycle. With deep domain expertise in regulatory sciences, clinical research solutions, quality & compliance, pharmacovigilance, medical information, and R&D technology, ProPharma offers an end-to-end suite of fully customizable consulting solutions that de-risk and accelerate our partners’ most high-profile drug and device programs.
Proteome Sciences is a CRO specialising in the analysis of proteins detected by Mass Spectrometry. We offer various Discovery and Targeted Services to characterise proteins and their associated post translational modifications. By using LC-MS2, SysQuant® and TMTcalibratorTM methodologies we can detect up to 8,000 of proteins/sample. With our proprietary bioinformatics software, these can be trimmed down to some tens of proteins that are either up-, or down-regulated with disease progression or drug treatment.
These key protein biomarkers can then be measured in a GCLP accredited Targeted Assay in a clinical trial, via a multiplexed assay of up to 100 proteins/sample.
New! We now offer Single Cell Proteome analysis.
New! We have just opened a full service lab in San Diego!
New! New services based on TMT-32 plex available now!
Back
Company Information
As for the company profile please use the following text: People Value Research (PVR) is a fast-responding and agile CRO, with a strong emphasis on quality and excellence in delivery. With operations across Europe, Israel, Ukraine, Georgia, and Türkiye, PVR combines global expertise with deep regional knowledge to accelerate drug development. In addition to our broad expertise, we have a strong focus on advanced therapies, including cell and gene therapies, biologics, and other innovative treatment modalities, supporting biotech, pharma, and medtech companies in navigating complex regulatory pathways and bringing breakthrough treatments to market.
Revvity Signals Software offers one of the most comprehensive arrays of scientific software in the world. Our powerful informatics solutions are used in many industries including Pharma and Biotech.
The needs of clinical researchers are complex, and clinical trials can generate vast amounts of critical data, but gleaning insights from this data is challenging for many organizations. To address this challenge, Revvity Signals has built Signals Clinical, powered by global analytics leader Spotfire®. Signals Clinical is a clinical data science solution that enables the delivery of insights to enhance study data quality, patient safety, and operations in near real-time to support workflows for clinical data review, medical review, clinical operations, risk-based monitoring, and pharmacovigilance.
No scientific company offers a wider range or more powerful solutions than Revvity Signals Software.
Rho, a contract research organization (CRO) located in Chapel Hill, NC, provides a full range of services across the entire drug development process. For more than 30 years, Rho has been a trusted partner to leading pharmaceutical, biotechnology, and medical device companies as well as academic and government organizations. Our commitment to excellence, innovative technologies, and therapeutic expertise accelerate time to market, maximize returns on investment, and lead to an exceptional customer experience.
ScienceMedia empowers biopharma, medtech, and CROs to embrace the science of learning and digital innovation to shorten trial timelines up to 20%, quicken site activations, save R&D spend, and propel therapeutic area training.
Our SMi TrialTM protocol compliance training solution eradicates protocol deviations and screening failures while reducing participant drop-outs and improving data quality.
Our SMi SourceTM cloud-based platform is a medically validated library of 400+ disease area and clinical science courses for learning and development across R&D, Clinical Operations, Medical Affairs, and Commercial organizations.
Scout empowers the life sciences industry with people-first solutions: Scout Meetings, Scout Clinical, and Scout Academy. We specialize in face-to-face, virtual, and hybrid clinical meeting planning, patient payment, travel, and logistics support, and virtual collaboration and education. Since 1995, we have been a trusted partner excelling in customer service, regulatory compliance, and project delivery for leading pharmaceutical and biotechnology companies. Our deep understanding of international regulations and adaptable network of resources is built on operational experience in 109 countries. With white-glove attention to detail and a customizable, comprehensive range of services, Scout makes the complex easier. Learn more at scoutclinical.com.
Back
Company Information
Sitero is a next-generation, clinical research partner that helps the life science industry get treatments to market safer and faster through tech-forward services that streamline research. Sitero’s clinical, eClinical, drug safety, biosafety, and ethical review services drive compliance and innovation for more than 200 customers worldwide.
Company Website
To learn more, please visit our website -
www.sitero.com
Back
Company Information
Syneos Health (Nasdaq:SYNH*) is the only fully integrated biopharmaceutical solutions organization. Our company, including a Contract Research Organization (CRO) and Contract Commercial Organization (CCO), is purpose-built to accelerate customer performance to address modern market realities. Created through the merger of two industry leading companies – INC Research and inVentiv Health – we bring together more than 21,000 clinical and commercial minds with the ability to support customers in more than 110 countries. Together, we share insights, use the latest technologies and apply advanced business practices to speed our customers’ delivery of important therapies to patients. To learn more about how we are shortening the distance from lab to lifeTM visit SyneosHealth.com.
TFS HealthScience is a global Contract Research Organization (CRO) partnering with biotechnology and pharmaceutical companies throughout their entire clinical development journey. Bringing together nearly 700 professionals, we deliver tailored clinical research services in more than 40 countries. TFS supports customers with comprehensive solutions including full clinical development services, strategic and flexible resourcing. In partnership, we build solution-driven teams of experienced professionals working together for a healthier future. Our mission is to bring treatments to patients faster. For more information, please visit www.tfscro.com.
Trialbee is the leading global data and technology platform for patient matching and enrollment in clinical trials. Partnering with sponsors, CROs, sites, and software providers, Trialbee is achieving patient enrollment goals and driving diversity in clinical trials. We are the smartest way to match and enroll patients for your clinical trial.
Company Website
To learn more, please visit our website -
trialbee.com
Back
Company Information
Putting patients first is in uMotif’s DNA. The uMotif eCOA/ePRO platform delivers faster, quality clinical trials and real-world studies by putting patients at the core of research. Through cloud-hosting in the US, Europe and China, the GCP, 21 CFR Part 11 and GDPR-compliant platform supports any study or trial, from Clinical Phase I, II and III studies through to decentralized or virtual real-world studies. Find out how uMotif can improve your clinical research programs and real-world studies at www.umotif.com
Company Website
To learn more, please visit our website -
www.umotif.com
Back
Company Information
Veramed is a pioneering CRO redefining intelligent healthcare decision-making through end-to-end biometrics that brings people, innovation, and technology together with world-class governance to accelerate evidence generation and advance patient health. With skilled Statisticians and Programmers uniquely matched and scaled to client needs, we produce exceptional deliverables swiftly using a blend of skill, rigorous governance, and automation to optimize the speed and success of clinical research from design and submission to launch and commercialization.
Versiti Clinical Trials Services support biopharma and cell therapy companies through central laboratory, logistics, biomaterials provision, and IRB services. We offer customizable specimen collection kits, specialty testing capabilities, dedicated project management and trial site support, biostorage, and real-time data management and reporting. Our Leukopaks are available for Research Use Only and Clinical Grade (FDA 21 CFR 1271-compliant) applications.
WCG measurably improves the quality and efficiency of clinical trials, helping biopharmaceutical companies, CROs, and institutions facilitate the development of new treatments and therapies for patients.
Back
Company Information
YPrime’s cloud-based technology streamlines clinical trial data collection and management. Electronic clinical outcome assessments (eCOA) and interactive response technology (IRT) platforms introduce greater speed, precision and data quality to clinical trials. Our consulting services help clients simplify downstream processes, while moving faster and more efficiently to their next development milestone.
We innovate through pragmatic, forward-looking change that considers the needs of stakeholders in each clinical research role. We’re doing more than streamlining your processes. We’re streamlining your research, helping you get to your next milestone faster.
Accelerate Recruitment Services specializes in patient recruitment for clinical trials, helping biopharma, CROs, and research sites connect with eligible participants. We go beyond traditional recruitment by collaborating with patient advocacy groups, building awareness before recruitment begins, and using creative strategies to ensure optimal enrollment. Our human-centric approach, combined with IRB-approved marketing, advanced pre-screening, and our TruView platform, streamlines enrollment, enhances engagement, and improves retention—accelerating recruitment timelines while keeping the patient experience at the forefront.
HeartcoR Solutions (HCS) is a leading Cardiac Safety Core Lab serving the Medical Device and Pharmaceutical Industries. HeartcoR has conducted 32 global IDE-PMA study projects since 2018 and has extensive understanding of Cardiac Safety execution to yield high study subject compliance in support of regulatory submissions. HCS’ also serves Bio-Pharmaceutical companies conducting intensive QT and phase I-IV safety studies. The Company’s 50 employees hold a required certifications and our Electrophysiologist/Cardiologist analysis team are recognized experts in heart rhythm analysis. HeartcoR is based in Schaumburg Illinois, twenty minutes north of O’Hare Airport.
Pharmaron’s Clinical Pharmacology Center (CPC) in Baltimore supports full-service early-phase clinical research for investigational products (IP). With 96-beds and access to a diverse population of healthy volunteers, our service achieves a 100% recruitment and 98% retention rate. Our expertise in First-In-Human studies in multiple therapeutic areas, especially infectious disease and vaccines, combined with our full suite of clinical pharmacology services, allows our team to advance drug development programs rapidly.
Worldwide is changing how the world experiences CROs – in the best possible way. From early phase, bioanalytical sciences, late phase, post-approval and real-world evidence, Worldwide Clinical Trials provides full-service drug development services for central nervous system, cardiovascular, metabolic, general medicine, oncology and rare disease therapies.
We work with you to design a bespoke package to meet your business needs, where you could:
Demonstrate your expertise on the agenda – have the attention of the entire audience. For greatest impact, why not position your talk before a networking break and immediately conduct follow up conversations with highly engaged attendees
Showcase your business and its services at an exhibition booth, which provides a perfect meeting place for prospective new clients
Present the value proposition of your offering over your competitors, in front of an audience of active, engaged potential customers
Speak with key decision makers as part of our intimate, interactive roundtable style workshop sessions with over 8 hours allowed for networking
Back
