27th Annual Clinical Trial Supply Europe 2026

2026 will see the return of the Clinical Trial Supply Europe conference to Barcelona where pharma, large and small, alongside biotechs will have the opportunity to discuss, debate and consider new technologies and processes to streamline supply chain operations. There’s never been a better time to exchange case studies, meet thought leaders, and discover the latest solutions from our selection of experienced exhibitors to create a robust clinical supply chain. Clinical Trial Supply Europe will be co-located with the & Temperature Controlled Logistics of Biopharmaceuticals Europe. It’s time to build relationships and take away valuable lessons for clinical trial success moving forward so we look forward to seeing you there!

24 - 25

February

2026
  • Barcelona
  • Complimentary
  • Why attend?
  • Agenda
  • Advisory Board
  • Speakers
  • Plan Your Visit
  • Event Gallery
  • Sponsors
  • Media Centre
  • Why partner?
  • CTS_TCL Session Slides
  • Contact Us
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2026 Sponsors Include:

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Company Information

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.

Company Website

To learn more, please visit our website - http://www.endpointclinical.com/

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Company Information

Clinical Services International (CSI) is a global leader of sourcing and management of commercially available medicines (comparators, concomitant medication) for clinical trials.
Headquartered in London and with operations in UK, Germany, Denmark, Japan and USA, we provide efficient solutions and serve worldwide trials. Our longstanding experience and relationships with manufacturers, enables us to provide custom made solutions to address the most complex requirements.
We accelerate drug development and reduce timelines by providing a fully integrated service.
Address Regulatory, Quality, Operational, Clinical requirements
Manage the entire supply chain and offer tailor-made solutions
Comprehensive expertise in Oncology and Biosimilar products.
Advanced Technology and Innovative approach
Trusted partner of leading Biopharmaceuticals, CROs and CMOs.
www.csint.com

Company Website

To learn more, please visit our website - www.csint.com

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Company Information

Founded in 1992, we are a privately owned clinical trial services company based in Kortrijk, Belgium.

 

We specialize in:

  • Customized Packaging & Labeling for IMPs and Auxiliary Medicines
  • QP Services, including GMP Audits of Manufacturing Sites outside the EEA
  • Global Distribution to Trial Sites
  • Sourcing of Commercial Medicines for Clinical Trial Use
  • Returns, Accountability & Destruction

To learn more, please visit our website – www.novitan.com

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Company Information

4G Clinical is a leader in randomization and trial supply management (RTSM) for the global life sciences industry, offering the only fully cloud-based, 100% configurable and flexible solution utilizing natural language processing (NLP) and integrated supply forecasting. 4G Clinical is headquartered in the Boston Biotech corridor of Wellesley, MA, with offices in Europe and Asia. For more information, please visit www.4gclinical.com

Company Website:http://www.4gclinical.com/

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Company Website

To learn more, please visit our website - www.expericservices.com

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Company Information

IMP Clinical Supply Services Ltd. specializes in local clinical trial supply chain management, offering tailored solutions including importation, QP release, packaging, storage, and distribution within Israel. With expertise in complex protocols and regulatory compliance, we ensure seamless logistics, rapid delivery, and high-quality service to support successful clinical trials locally.

Company Website

To learn more, please visit our website - https://imp-services.co.il/

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For more than 35 years, Swiss-based ELPRO, part of the Bosch Group, is a global solution provider for innovative environmental monitoring for the pharmaceutical, life science, biotech, and health care industries. Technology based services, state-of-the-art data loggers, SaaS software platforms including data analytics, and GxP experts to support the system integration into your business processes, ensure efficiency and compliance throughout your supply chain. Our PDF data loggers for rooms and transports measure temperatures from -200 °C to +200 °C. They do not require any hardware or software to install or validate. Thanks to innovative service models and cloud-based database solutions, our customers always have the right GxP-compliant monitoring solution for every application. ELPRO is ISO 9001 certified, operates ISO 17025 accredited laboratories according to SCS/NIST, and adheres to GAMP® 5 guidelines. Sales and technical support offices are located in Switzerland, US, Canada, UK, Germany, the Nordics, Benelux, Singapore, and Japan.

For more information, visit ELPRO.com.

Company Website

To learn more, please visit our website - http://www.elpro.com/

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Company Information

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.

We’ve been delivering care for 17 years: https://oximio.com/

Company Website

To learn more, please visit our website - www.oximio.com

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Company Information

Complex innovative clinical trial designs require a synergetic approach to assess novel drug compounds for safety and effectiveness which often span safety, regulated and esoteric outcomes in all phases of the drug development life cycle. The companies of Eurofins Bioanalytical Services, the Eurofins Central Laboratory global network, Eurofins Viracor BioPharma Services, and Eurofins Clinical Trial Supplies are strongly connected to provide a solutions-based approach to our client needs.  Eurofins Clinical Trial Solutions provides seamless, end-to-end solutions to help clients progress through the drug development cycle through a single, experienced provider. Our solutions deliver the most comprehensive range of state-of-the-art analytical technologies with an extensive geographic reach to support our clients’ testing and clinical supplies needs and stringent quality and safety requirements around the world.

Company Website

To learn more, please visit our website - https://www.eurofins.com/biopharma-services/clinical-trial-solutions/

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Company Information

N-SIDE is a deeptech company that empowers organizations in the life sciences to make better decisions and optimize the use of critical resources. We’re doing so by combining deep industry expertise with applied mathematics and artificial intelligence into easy to use and cutting-edge software that transforms uncertainty and complexity into deterministic outcomes. We are an active player in clinical trial supply chain management for over 20 years and have the majority of the top 20 pharmaceutical companies as clients.

With our software solution, the N-SIDE Suite, and expert services, we streamline the clinical supply of pharmaceutical and biotech companies by accelerating clinical plans, mitigating risks and curbing drug waste. We empower clinical leaders to make better, faster and safer decisions for patients waiting for life-changing medications.

Company Website

To learn more, please visit our website - https://lifesciences.n-side.com/

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Company Information

Suvoda is a global clinical trial technology company specializing in complex, life-sustaining studies in therapeutic areas like oncology, central nervous system (CNS), and rare disease. Founded in 2013 by experts in eClinical technologies, Suvoda empowers clinical trial professionals to manage the most urgent moments in the most urgent trials through advanced software solutions delivered on a single platform. Headquartered outside Philadelphia, Suvoda also maintains offices in Portland, OR, Barcelona, Spain, Bucharest and Iasi, Romania, and Tokyo, Japan. The company’s Net Promoter Score (NPS) consistently exceeds the technology industry average, contributing to the company being selected by trial sponsors and CROs to support more than 1,000 trials across 80 countries.

Company Website

To learn more, please visit our website - https://www.suvoda.com/

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Medidata is powering smarter treatments and healthier people through digital solutions to support clinical trials. Celebrating 25 years of ground-breaking technological innovation across more than 35,000 trials and 10 million patients, Medidata offers industry-leading expertise, analytics-powered insights, and the largest patient-level historical clinical trial data set in the world. More than 1 million registered users across approximately 2,300 customers trust Medidata’s seamless, end-to-end platform to improve patient experiences, accelerate clinical breakthroughs, and bring therapies to market faster. A Dassault Systèmes brand (Euronext Paris: FR0014003TT8, DSY.PA), Medidata is headquartered in New York City and has been recognized as a Leader by Everest Group and IDC. Discover more at www.medidata.com and follow us @Medidata.

Company Website

To learn more, please visit our website - https://www.medidata.com

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Company Information

Transform the way you look at drug distribution across the clinical supply chain!

Our world-leading cloud temperature management solution is designed with pharma – for pharma. It enables you to meet compliance, identify lean and sustainable initiatives in the supply chain, and ultimately deliver drugs safely.​

Company Website

To learn more, please visit our website - http://www.tss.se/

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DHL Life Sciences & Healthcare offers a comprehensive global logistics portfolio that is designed to meet the specific needs and challenges of the industry, with worldwide network operations, rigorous clinical and pharmaceutical governance, and incorporating high environmental standards. The DHL global clinical logistics network connects tens of thousands of researchers, sponsors, and patients with compliant, safe, and robust distribution systems.  Clinical trials logistics professionals can take advantage of these established, trusted DHL networks to reach out to patients, laboratories, and researchers across the world. DHL delivers the vital logistics that ensure clinicians and researchers can complete their work, improving health outcomes for all.

Company Website

To learn more, please visit our website - http://www.logistics.dhl/global-en/home/our-divisions/supply-chain/sectors-overview/life-sciences-and-healthcare/our-life-sciences-and-healthcare-expertise.html

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Company Information

Inthera is a European family-owned pharmaceutical wholesaler specializing in supplying various original, biosimilar and generic medicines for clinical trials worldwide. Thanks to our decades long experience we have access to a vast portfolio of medicines confirming to the highest standards from various manufacturers, with flexible pricing and short delivery times.

Company Website

To learn more, please visit our website - http://inthera.net

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Company Website

To learn more, please visit our website - www.tempmate.com

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Signant Health provides solutions that simplify every step of the patient journey to make it easier for people to participate in, and for sites and study teams to run, clinical trials. Signant unites eCOA, eConsent, Patient Engagement, IRT, Clinical Supplies and Endpoint Quality into the industry’s most comprehensive patient-centric suite – an evolution built on more than 20 years of proven clinical research technology. Our intense focus on the patient experience, deep therapeutic area expertise and global operational scale enable hundreds of sponsors and CROs (including all Top 20 pharma) to extend the reach of drug development, expand patient opportunities and improve data quality – helping them bring life-changing therapies to our families and communities around the world.

Company Website

To learn more, please visit our website - www.signanthealth

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Company Information

Akesa is an end-to-end provider of clinical trial supplies and services. Headquartered in Melbourne, Australia, Akesa boasts global reach with deep expertise in the Asia-Pacific region. We work alongside sponsors, CROs, research institutions, clinical trial sites and CDMOs to project manage the sourcing of finished products, including comparators, combination therapies, and standard-of-care medications, from validated suppliers and directly from manufacturers.

Company Website

To learn more, please visit our website - http://akesapharma.com/

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Company Information

With 35 years of experience, a global network of 30 purpose-built cGMP facilities and end to end capabilities across IMP, demand planning, comparator, ancillaries, packaging, labeling, cold chain and distribution Thermo Fisher Scientific clinical supply has the capacity, stability, expertise and global supply chain to support your project today. Additionally, being an integrated CRO and CDMO Thermo Fisher Scientific has the unique ability to support you from clinical research and clinical manufacturing through to clinical supply and execution.

Company Website

To learn more, please visit our website - https://url.uk.m.mimecastprotect.com/s/ceBZCvQgLukWow3hXh0IQ1rns?domain=patheon.com

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Company Information

We acknowledge that your products are highly sensitive to temperature and need strictly controlled shipping solutions.

T°Safe’s precise planning, careful risk assessment and rigorous performance ensures a high quality supply chain of API and an effective, IT-powered (iDEX) clinical trial distribution of IMP. This is key for a successful partnership with our customers.

Company Website

To learn more, please visit our website - http://www.tsafelogistics.com/

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    Why attend?

    2026 will see the return of the Clinical Trial Supply Europe conference to Barcelona where pharma, large and small, alongside biotechs will have the opportunity to discuss, debate and consider new technologies and processes to streamline supply chain operations.

    There’s never been a better time to exchange case studies, meet thought leaders, and discover the latest solutions from our selection of experienced exhibitors to create a robust clinical supply chain.

    Clinical Trial Supply Europe will be co-located with the & Temperature Controlled Logistics of Biopharmaceuticals Europe.

    It’s time to build relationships and take away valuable lessons for clinical trial success moving forward so we look forward to seeing you there!

    WHAT TO EXPECT FOR 2025?

    Clinical Trial Supply Europe is the meeting place for the pharmaceutical and biotechnology community to discover how to excel in clinical supply strategy as well as form key connections for long-term success.

    500+

    Attendees

    		55+

    Exhibitors

    		30+

    Speakers
    500+

    Attendees

    		55+

    Exhibitors
    30+

    Speakers

    Testimonials

    See What It's All About

    Agenda

    • 24 Feb 2026
    • 25 Feb 2026
    Expand All

    Streams

    Stream one

    Clinical Supply Logistics and Operations

    Stream two

    Clinical Supply Technology and Innovation

    11 AM

    Case Study: Harnessing use of AI to assist throughout clinical supply chain

    • Discovering how AI is transforming pharmaceutical supply chains beyond traditional automation
    • Revealing how intelligent systems revolutionize forecasting, operations, quality management, and project coordination
    • Learning the practical journey from basic automation to AI-powered insights that drive measurable business outcomes across the
      clinical supply chain

    Speakers

    Landry Giardina
    Global Head of Clinical Supply Chain Operations, Innovation & Technology, Sanofi

    11:30 AM

    Reserved for Mercalis

    12 PM

    Transforming pharmaceutical operations and supply chain through intelligent automation: AI in action!

    • AI-powered demand forecasting
    • Dynamic logistics optimization
    • Proactive inventory management
    • AI agents in the supply chain

    Speakers

    Doron Azran
    VP Supply Chain & CPO, SK Pharma

    12:30 PM

    Reserved for S-CLINICA

    1 PM

    Lunch and networking

    2 PM

    Driving digital transformation across regulatory, manufacturing and supply chain

    Speakers

    Monitha Harilkumar
    Director Data & Digital Acceleration Lead, Roche

    2:30 PM

    Reserved for CCL Clinical

    3 PM

    Strategies and solutions to overcome drug supply shortages

    • Monitoring global manufacturing bottlenecks due to raw material shortages and geopolitical instability
    • Using adaptive supply forecasting to avoid over or under forecasting
    • Considering regulatory and logistic hurdles such as customs delays and cold chain failures
    • Using drug pooling to ensure continuity of supply

    Speakers

    Manfredi Punginelli
    Senior Manager Global Clinical Supply, Incyte

    3:30 PM

    Afternoon refreshments and networking

    4 PM

    Panel Discussion: Innovating in clinical supply through new technology and strategy

    • Incorporating digitalization and new technologies into your clinical trial supply chain
    • Collaborative platforms: improving communication and efficiency among stakeholders
    • Success stories, transformative case studies and key takeaways
    • Looking to the future: where do we expect to be in 5 years’ time with advancing technologies?

    4:45 PM

    Reserved for event sponsor

    7:30 AM

    Registration and refreshments

    8:15 AM

    Chairperson’s opening remarks

    8:30 AM

    Opening Keynote: Leading the transformation: future of clinical supply chain models to maintain adaptability and flexibility

    • Adapting supply models to meet increasing patient centric trial approaches
    • Incorporating advances in technology and digital tools
    • Raising efficiency and sustainability measures to streamline supply and reduce waste
    • Remaining flexible, responsive, and capable of supporting the diverse needs of modern research

    Speakers

    Arnaud Dourlens
    Global Head of Clinical Supply Chain Operations, Sanofi

    9 AM

    Reserved for Suvoda

    9:30 AM

    Panel Discussion: Forging strong relationships and communication strategies as a clinical supply professional to enhance trial resilience and success

    • Breaking down silos to include clinical supply in other departmental discussions earlier
    • Bridging the gap between clinical supply, CMC, quality, clinical operations and other stakeholders
    • Utilizing robust relationships to be better prepared when running into problems conducting trials
    • Increasing the resilience of your trial through succinct collaboration

    Speakers

    Luiz Barberini
    Head of External Manufacturing, Latin America, Bayer
    Sanae Zahraoui
    Supply Chain Manager, TILT Biotherapeutics

    10 AM

    Reserved for TSS

    10:30 AM

    Morning refreshments and networking

    11 AM

    Overcoming Import of Record and distribution challenges in clinical supplies

    • Finding a vendor who can be your importer of record
    • Understanding packaging and labelling differences between countries
    • Reviewing if and when you can reclaim VAT: which European countries support reclaiming R&D activities
    • Considering advantages of a central distribution model vs standard local model

    Speakers

    Maite Montes Vallina
    Head of Clinical Supply Partnering, UCB

    11:30 AM

    Reserved for DHL

    12 PM

    From source to site: navigating clinical supply vendors and logistics

    • Managing logistics and distribution effectively and efficiently
    • Determining criteria for vendor selection
    • Overcoming the complexities of comparator sourcing

    Speakers

    Kyrillos Sarigiannidis
    Head of Drug Supply, Affimed

    12:30 PM

    Reserved for Oximio

    1 PM

    Lunch and networking

    2 PM

    Outsourcing comparator sourcing effectively to ensure timely acquisition of supplies

    • Selecting a provider: considering size and location of trial, quality assurance, regulatory expertise and ability to ensure consistent supply throughout trial
    • Balancing cost effectiveness with risk management: transparent pricing models, supply chain visibility and contingency plans for disruptions or shortages
    • Oversight of comparator sourcing partner: maintaining compliance across different regions and aligning with trial specific protocols

    Speakers

    Michelle Divine
    Head of Clinical Trial Supply Management, LEO Pharma

    2:30 PM

    Reserved for ALMAC

    3 PM

    Case Study: Sharing clinical supply processes and challenges within a complex cell therapy trial

    • Understanding and complying with regulation to limit delays
    • Choosing a manufacturing and distribution model to suit trial supply
    • Considering temperature monitoring and control options to reduce excursions and waste
    • Reviewing challenges faced and lessons learnt

    Speakers

    Elvira Tejedor
    End to End Supply Planner, Takeda

    3:30 PM

    Afternoon refreshments and networking

    4 PM

    Panel Discussion: Navigating complexities when shipping IMPs

    • Overcoming regulatory and compliance hurdles
    • Ensuring packaging and labelling meets country specific requirements
    • Considering solutions for temperature control management during shipping
    • Coordinating between depots, CROs, carriers and sites

    Speakers

    Sanae Zahraoui
    Supply Chain Manager, TILT Biotherapeutics
    Ana-Zeralda Canals Hamann
    Associate Director Clinical Trial Supplies, Debiopharm

    4:45 PM

    Reserved for event sponsor

    5:15 PM

    Closing Keynote: Evaluating clinical supply processes and challenges across the pharma industry

    • Sharing industry benchmarking outcomes
    • Considering synergy opportunities
    • Highlighting key challenges for the next 5 years

    Speakers

    Landry Giardina
    Global Head of Clinical Supply Chain Operations, Innovation & Technology, Sanofi

    5:35 PM

    Chairperson’s closing remarks

    END OF DAY 1 AND NETWORKING DRINKS

    Streams

    Stream one

    Clinical Supply Logistics and Operations

    Stream two

    Clinical Trial Supply Technology & Innovation

    8:55 AM

    Chairperson’s opening remarks

    9 AM

    Keynote Case Study: Enhancing clinical supply chains with cutting-edge drone technology

    • Leveraging drone technology to overcome logistical challenges and improve access to healthcare in remote and rural areas
    • Reducing delivery times for critical materials from several hours to 30 minutes, enabling smarter, more efficient clinical trial supply chains
    • Enhancing patient care and increasing diversity with accessibility for those in remote locations
    • Sharing the broader impact on healthcare supply chains

    Speakers

    Samantha Carmichael
    Lead Pharmacist Clinical Trials, NHS Greater Glasgow and Clyde
    Katriona Brooksbank
    Innovation Lead, NHS Greater Glasgow and Clyde

    9:30 AM

    Reserved for event sponsor

    10 AM

    Focusing on patient centricity within packaging, labelling and e-labelling labelling strategy

    • Working with patient experts to gain their feedback and insight on packaging and labelling
    • Raising awareness of patient voice within CMC
    • Improving accessibility for labels and IFU
    • e-labelling and how to better use it as a tool
    • Gathering patient feedback at end of study

    Speakers

    Amanda Briceno
    Clinical Supply Management & Patient Centricity Unit Manager, Chiesi Farmaceutici

    10:30 AM

    Reserved for event sponsor

    11 AM

    Morning refreshments and networking

    11:45 AM

    Sharing systems and processes for measuring sustainability and green in supply chain

    • Focusing on how enterprise level integration brings advantages in inventory and supply management
    • Calculating and reporting Co2 emissions for forecast and actuals
    • Leveraging Co2 emission data for trial distribution network design
    • Discussing challenges and future ambition on overage/coverage calculation, reporting per study and waste reduction

    Speakers

    Loris Sainlez
    Clinical Supply Performance System Lead, UCB

    12:15 PM

    Reserved for event sponsor

    12:45 PM

    Panel Discussion: Establishing a robust forecasting strategy to minimize cost and waste

    • Implementing a robust forecasting strategy to optimize clinical supply chain management
    • Analysing data to predict trends and accurately forecast supply chain needs
    • Harnessing technology to assist with effective forecasting and reduce waste
    • Establishing open communication with CROs to enhance forecasting

    Speakers

    Kamal Amin
    Head of Clinical Supplies Management, Galderma

    8:15 AM

    Registration and refreshments

    8:55 AM

    Chairperson’s opening remarks

    9 AM

    Keynote Fireside Chat: Securing your supply chain: managing and preparing for risk amidst geopolitical changes

    • Designing an adaptable supply chain to remain agile in the face of disruptions
    • Leveraging technologies to improve your visibility and end to end supply chain
    • Incorporating risk assessment and building contingency protocols early to be more prepared
    • Learning on the go and acting fast as new challenges appear

    Speakers

    Kamal Amin
    Head of Clinical Supplies Management, Galderma

    9:30 AM

    Reserved for event sponsor

    10 AM

    Managing CMO vendors to ensure an effective partnership

    • Agreeing timelines and establishing your oversight requirements
    • Creating feedback and performance review processes to manage partnerships
    • Fostering effective communication and collaboration to form strong relationships

    Speakers

    Philip Coetzee
    Director CMO Management, Daiichi Sankyo

    10:30 AM

    Reserved for event sponsor

    11 AM

    Morning refreshments and networking

    11:45 AM

    Selecting, managing and oversight of clinical supply vendors

    • Establishing a selection process and criteria for choosing vendors
    • Building and managing relationships to ensure good communication lines
    • Agreeing timelines and establishing your oversight requirements

    Speakers

    Neil Fox
    Director Clinical Supplies, CellCentric

    12:15 PM

    Reserved for event sponsor

    12:45 PM

    Understanding duty rate and entry rates in US clinical supply chain imports

    • Classifying clinical materials correctly to avoid delays or unexpected costs
    • Collaborating with brokers and logistics partners to ensure compliant, efficient importation
    • Determining duty rates and entry rates for different types of clinical trial materials and products
    • Applying for duty exemptions: are you eligible?

    U.S. Customs and Border Protection (Provisionally confirmed)

    1:15 PM

    Lunch, networking and prize draw

    2:30 PM

    ROUNDTABLE SESSIONS

    During the roundtable discussion session, the conference hall will be divided into zones. Delegates can choose which zone they would like to join. Each zone will be led by a table moderator and will focus on a different challenge within the industry. After 45 minutes, delegates will have the opportunity to swap and choose a different table, and each roundtable will run twice

    Roundtable 1: Meeting sustainability targets for pharma supply chains
    Kamal Amin, Head of Clinical Supplies Management, Galderma

    Roundtable 2: Managing supply chain vendors to ensure smooth logistical operations
    Luiz Barberini, Head of External Manufacturing, Latin America, Bayer

    Roundtable 3: Topic TBC
    Chiara Venuti, Member of the Management Board, Cool Chain Association

    Roundtable 4: Incorporating digitalization, AI and new technologies into your clinical trial supply chain

    Roundtable 5: Executing a direct to patient trial successfully within Europe

     

    Speakers

    Kamal Amin
    Head of Clinical Supplies Management, Galderma
    Luiz Barberini
    Head of External Manufacturing, Latin America, Bayer
    Chiara Venuti
    Member of the Management Board, Cool Chain Association

    END OF CONFERENCE

    Speakers

    Select a speaker to learn more

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    Kyrillos Sarigiannidis
    Head of Drug Supply, Affimed

    Session Details:

    From source to site: navigating clinical supply vendors and logistics

    2026-02-24, 12:00 PM

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    Luiz Barberini
    Head of External Manufacturing, Latin America, Bayer
    • Over 25 years’ experience in Logistics, Supply Chain, Procurement and Demand Planning areas.
      Solid knowledge and experience in the whole S&OP process and its KPI´s inter-relationships with stakeholders
    • Demand Planning process management - pre-S&OP, with Sales, Marketing, Trade Marketing, Industrial Planning and Finance and customized tool design for such process
    • Management skills: experience with multidisciplinary and international teams (Brazil / Latin America / US).
    • Experience in S&OP, 3PL and Supply Chain Organization projects' implementation
    • Strong experience with Pharmaceutical and Consumer companies and Brazilian distribution model / 3PL contracts
    • Solid team management skills, as well as Customer Service relationship and management
    • Teacher for major Post Graduation Schools - Demand Planning and Procurement/Negotiation areas

    CSCP & CPIM APICS. Logistics & Supply Chain driven strategy. Distribution & Logistics, Demand Planning, S&OP, Procurement and Export experiences, focusing on Business necessities through effective leadership.

    Working as External Manufacturing Operations Manager Latin America at Bayer, in charge for external partners for CHC Division. Previously as Relationship Associated Director at Merck , Logistics Manager at Takeda/Nycomed Pharma, focusing on demand management, planning and distribution activities. Also has worked as Pfizer´s Logistic Manager and EFD´s Supply Chain Manager. Souza Cruz´s Procurement Manager and Rhodia's Logistic Supervisor.

    Specialties: Logistics, Supply Chain, Materials, Procurement , Services, Negotiation, 3PL contracts, S&OP, Demand Planning

    Session Details:

    ROUNDTABLE SESSIONS

    2026-02-25, 2:30 PM

    Session Details:

    Panel Discussion: Forging strong relationships and communication strategies as a clinical supply professional to enhance trial resilience and success

    2026-02-24, 9:30 AM

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    Neil Fox
    Director Clinical Supplies, CellCentric

    Session Details:

    Selecting, managing and oversight of clinical supply vendors

    2026-02-25, 11:45 AM

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    Amanda Briceno
    Clinical Supply Management & Patient Centricity Unit Manager, Chiesi Farmaceutici

    Amanda Briceno is an experienced clinical supply professional with over 10 years in clinical research and supply chain operations. Originally from Venezuela, now based in Italy. She currently serves as Clinical Supply Manager and Head of the Patient Centricity Unit at Chiesi Farmaceutici, where she leads initiatives to design and deliver patient-focused clinical supply solutions that improve trial compliance and enhance the experience of both patients and site staff.

    Her career began as a Clinical Research Associate at IQVIA, where she gained extensive experience in global trial monitoring and operations. Since joining Chiesi, Amanda has held positions of increasing responsibility within the Clinical Supply department, before assuming her current leadership role.

    Amanda holds a Master’s degree in Drug Biotechnology from the Università degli Studi di Milano and a Bachelor’s degree in Medical Biotechnology. Amanda brings a strong blend of technical knowledge and operational leadership. Passionate about innovation in clinical supplies, she is dedicated to advancing more accessible, patient-centric clinical trials.

    Session Details:

    Focusing on patient centricity within packaging, labelling and e-labelling labelling strategy

    2026-02-25, 10:00 AM

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    Chiara Venuti
    Member of the Management Board, Cool Chain Association

    Session Details:

    ROUNDTABLE SESSIONS

    2026-02-25, 2:30 PM

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    Philip Coetzee
    Director CMO Management, Daiichi Sankyo

    Session Details:

    Managing CMO vendors to ensure an effective partnership

    2026-02-25, 10:00 AM

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    Ana-Zeralda Canals Hamann
    Associate Director Clinical Trial Supplies, Debiopharm

    Session Details:

    Panel Discussion: Navigating complexities when shipping IMPs

    2026-02-24, 4:00 PM

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    Manfredi Punginelli
    Senior Manager Global Clinical Supply, Incyte

    Session Details:

    Strategies and solutions to overcome drug supply shortages

    2026-02-24, 3:00 PM

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    Kamal Amin
    Head of Clinical Supplies Management, Galderma

    Kamal is a trained Chemist who decided to pursue a career in supply chain management and quality. In this role, he was tasked to supervise commercial and clinical trial products. Kamal has worked in the pharmaceutical and device industries for over 15 years in different size organisations ranging from large multinational to small virtual companies. He is currently leading a global team at Galderma to develop an integrated clinical supply chain organisation within the company.

    Session Details:

    Keynote Fireside Chat: Securing your supply chain: managing and preparing for risk amidst geopolitical changes

    2026-02-25, 9:00 AM

    Session Details:

    Panel Discussion: Establishing a robust forecasting strategy to minimize cost and waste

    2026-02-25, 12:45 PM

    Session Details:

    ROUNDTABLE SESSIONS

    2026-02-25, 2:30 PM

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    Michelle Divine
    Head of Clinical Trial Supply Management, LEO Pharma

    Session Details:

    Outsourcing comparator sourcing effectively to ensure timely acquisition of supplies

    2026-02-24, 2:00 PM

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    Samantha Carmichael
    Lead Pharmacist Clinical Trials, NHS Greater Glasgow and Clyde

    Session Details:

    Keynote Case Study: Enhancing clinical supply chains with cutting-edge drone technology

    2026-02-25, 9:00 AM

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    Katriona Brooksbank
    Innovation Lead, NHS Greater Glasgow and Clyde

    Session Details:

    Keynote Case Study: Enhancing clinical supply chains with cutting-edge drone technology

    2026-02-25, 9:00 AM

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    Monitha Harilkumar
    Director Data & Digital Acceleration Lead, Roche

    Session Details:

    Driving digital transformation across regulatory, manufacturing and supply chain

    2026-02-24, 2:00 PM

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    Arnaud Dourlens
    Global Head of Clinical Supply Chain Operations, Sanofi

    Arnaud Dourlens is an Arts et Métiers engineer, he began his industrial career in the FMCG sector where he held growing responsibilities. Then he joined the LVMH group where he reorganized new product launches and industrial investments in the Make-up segment in order to adapt to the need for innovation and time to market, thus providing a competitive advantage. He then managed the entire portfolio of industrial launches and investments in Perfumes, Skincare and Make-up for Parfums Christian Dior Group.

    During his career Arnaud held a wide variety of industrial roles. He joined Sanofi in 2017 as Production Director of a major solid oral form production site (>2.5 billion € turnover). He has been a key player in the development of the continuous improvement mindset and in the transformation of the site through IT projects, investments and activity growth following the acquisition of Boehringer Ingelheim consumer healthcare portfolio.

    Since the beginning of 2020, he’s been the global head of Sanofi Clinical Supply Chain Operations, managing worldwide clinical supply teams involved in more than 300 clinical studies.

    Session Details:

    Opening Keynote: Leading the transformation: future of clinical supply chain models to maintain adaptability and flexibility

    2026-02-24, 8:30 AM

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    Landry Giardina
    Global Head of Clinical Supply Chain Operations, Innovation & Technology, Sanofi

    20y+ experience within pharmaceutical industry and specially within clinical supply chain, Digital development, and innovation.

    Career started as a biochemist engineer, Landry has moved progressively to drug manufacturing process development, GMP production, comparator supply & material flow management and then innovation and technology for clinical supplies.

    Key drivers of his career are continuous improvement, factual based decision and valuable innovation implementation.

    Session Details:

    Closing Keynote: Evaluating clinical supply processes and challenges across the pharma industry

    2026-02-24, 5:15 PM

    Session Details:

    Case Study: Harnessing use of AI to assist throughout clinical supply chain

    2026-02-24, 11:00 AM

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    Doron Azran
    VP Supply Chain & CPO, SK Pharma

    Session Details:

    Transforming pharmaceutical operations and supply chain through intelligent automation: AI in action!

    2026-02-24, 12:00 PM

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    Elvira Tejedor
    End to End Supply Planner, Takeda

    Session Details:

    Case Study: Sharing clinical supply processes and challenges within a complex cell therapy trial

    2026-02-24, 3:00 PM

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    Sanae Zahraoui
    Supply Chain Manager, TILT Biotherapeutics

    Session Details:

    Panel Discussion: Navigating complexities when shipping IMPs

    2026-02-24, 4:00 PM

    Session Details:

    Panel Discussion: Forging strong relationships and communication strategies as a clinical supply professional to enhance trial resilience and success

    2026-02-24, 9:30 AM

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    Loris Sainlez
    Clinical Supply Performance System Lead, UCB

    Session Details:

    Sharing systems and processes for measuring sustainability and green in supply chain

    2026-02-25, 11:45 AM

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    Maite Montes Vallina
    Head of Clinical Supply Partnering, UCB

    Session Details:

    Overcoming Import of Record and distribution challenges in clinical supplies

    2026-02-24, 11:00 AM

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    Advisory Board

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    Chris Wallace
    Head of Distribution EMEA, Argenx

    Chris has over 35 years’ varied supply chain experience, having worked for several blue chip companies in a number of industries including 3rd party logistics services, automotive, medical device, nuclear fuels and biotech/pharmaceuticals.

    Originally from the UK but now based in Switzerland, he has been involved in life science - biotech/pharmaceuticals & medical device - for over 20 years of his career and has latterly been SVP Global Supply Chain at Clover Biopharmaceutical before last year moving to Argenx as Head of Distribution EMEA.

    He has developed, implemented and managed global healthcare supply chain strategies and operations on 6 continents. This has included different set-ups in multiple countries, including many in the Emerging Markets as well as the developed world.

    Chris has a degree in economics from Manchester University, an MBA from Aston University and a postgraduate diploma from London University. In his spare time, he plays golf badly and loves to sample great Italian food and red wines!

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    Luiz Barberini
    Head of External Manufacturing, Latin America, Bayer
    • Over 25 years’ experience in Logistics, Supply Chain, Procurement and Demand Planning areas.
      Solid knowledge and experience in the whole S&OP process and its KPI´s inter-relationships with stakeholders
    • Demand Planning process management - pre-S&OP, with Sales, Marketing, Trade Marketing, Industrial Planning and Finance and customized tool design for such process
    • Management skills: experience with multidisciplinary and international teams (Brazil / Latin America / US).
    • Experience in S&OP, 3PL and Supply Chain Organization projects' implementation
    • Strong experience with Pharmaceutical and Consumer companies and Brazilian distribution model / 3PL contracts
    • Solid team management skills, as well as Customer Service relationship and management
    • Teacher for major Post Graduation Schools - Demand Planning and Procurement/Negotiation areas

    CSCP & CPIM APICS. Logistics & Supply Chain driven strategy. Distribution & Logistics, Demand Planning, S&OP, Procurement and Export experiences, focusing on Business necessities through effective leadership.

    Working as External Manufacturing Operations Manager Latin America at Bayer, in charge for external partners for CHC Division. Previously as Relationship Associated Director at Merck , Logistics Manager at Takeda/Nycomed Pharma, focusing on demand management, planning and distribution activities. Also has worked as Pfizer´s Logistic Manager and EFD´s Supply Chain Manager. Souza Cruz´s Procurement Manager and Rhodia's Logistic Supervisor.

    Specialties: Logistics, Supply Chain, Materials, Procurement , Services, Negotiation, 3PL contracts, S&OP, Demand Planning

    Session Details:

    ROUNDTABLE SESSIONS

    2026-02-25, 2:30 PM

    Session Details:

    Panel Discussion: Forging strong relationships and communication strategies as a clinical supply professional to enhance trial resilience and success

    2026-02-24, 9:30 AM

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    Amanda Briceno
    Clinical Supply Management & Patient Centricity Unit Manager, Chiesi Farmaceutici

    Amanda Briceno is an experienced clinical supply professional with over 10 years in clinical research and supply chain operations. Originally from Venezuela, now based in Italy. She currently serves as Clinical Supply Manager and Head of the Patient Centricity Unit at Chiesi Farmaceutici, where she leads initiatives to design and deliver patient-focused clinical supply solutions that improve trial compliance and enhance the experience of both patients and site staff.

    Her career began as a Clinical Research Associate at IQVIA, where she gained extensive experience in global trial monitoring and operations. Since joining Chiesi, Amanda has held positions of increasing responsibility within the Clinical Supply department, before assuming her current leadership role.

    Amanda holds a Master’s degree in Drug Biotechnology from the Università degli Studi di Milano and a Bachelor’s degree in Medical Biotechnology. Amanda brings a strong blend of technical knowledge and operational leadership. Passionate about innovation in clinical supplies, she is dedicated to advancing more accessible, patient-centric clinical trials.

    Session Details:

    Focusing on patient centricity within packaging, labelling and e-labelling labelling strategy

    2026-02-25, 10:00 AM

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    Paul Hingst
    Supply Chain Consultant, Crinetics Pharmaceuticals

    Paul is an experienced Clinical Supply Chain Professional with a 25-year career in the BioPharmaceutical industry.  His extensive career includes roles at major companies like Amgen and Thermo Fisher Scientific, where he honed his skills and made a significant impact.  He has served in varied roles from basic research and contract manufacturing to client services and account management.  He is a Principal Consultant and Co-Founder of Beacon BioPharm Associates, a clinical supply chain consulting firm, providing variable staffing solutions to small and mid-sized BioPharm clients.  Paul is an industry veteran and respected leader known for his expertise in clinical supply chain.

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    Amaury Jeandrain
    Strategy Advisor, Clinical Supply, N-SIDE

    Amaury Jeandrain has a Master’s Degree in Business Engineering with a specialization in supply chain optimization. He joined Clinigen in 2015, then N-SIDE in 2016 where he last  held the position of VP of Strategy for clinical supply solutions.

    Over the past decade, his objective has been to make clinical trial supply chains more efficient by redefining CTS strategies and driving measurable performance improvements. His expertise also includes forecasting, planning, waste reduction, and shortage risk mitigation.

    Since 2024, while accompanying his wife on humanitarian missions abroad (Niger, then Colombia), Amaury has continued his work as a CTS advisor and trainer, partnering with pharmaceutical companies worldwide to enhance clinical supply performance.

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    Francesco Santo
    Director Clinical Supply Chain,
    Orano Med

    A highly experienced and passionate Director Clinical Supply Chain, Francesco has dedicated the past 17 years to ensuring the seamless execution of clinical trials by optimizing supply chain operations. His deep commitment to this field is driven by a relentless pursuit of excellence in delivering life-saving treatments to patients worldwide.  Throughout his career, he has honed a diverse skill set, encompassing:

    • Strategic Supply Chain Management
    • Regulatory Compliance
    • Cross-Functional Collaboration
    • Risk Management
    • Innovative Problem-Solving

    Francesco’s dedication to the clinical supplies industry is rooted in a profound understanding of the critical role it plays in advancing medical research and improving patient outcomes. He is committed to continuing his journey in this field, always striving to contribute to the betterment of global health.

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    Arnaud Dourlens
    Global Head of Clinical Supply Chain Operations, Sanofi

    Arnaud Dourlens is an Arts et Métiers engineer, he began his industrial career in the FMCG sector where he held growing responsibilities. Then he joined the LVMH group where he reorganized new product launches and industrial investments in the Make-up segment in order to adapt to the need for innovation and time to market, thus providing a competitive advantage. He then managed the entire portfolio of industrial launches and investments in Perfumes, Skincare and Make-up for Parfums Christian Dior Group.

    During his career Arnaud held a wide variety of industrial roles. He joined Sanofi in 2017 as Production Director of a major solid oral form production site (>2.5 billion € turnover). He has been a key player in the development of the continuous improvement mindset and in the transformation of the site through IT projects, investments and activity growth following the acquisition of Boehringer Ingelheim consumer healthcare portfolio.

    Since the beginning of 2020, he’s been the global head of Sanofi Clinical Supply Chain Operations, managing worldwide clinical supply teams involved in more than 300 clinical studies.

    Session Details:

    Opening Keynote: Leading the transformation: future of clinical supply chain models to maintain adaptability and flexibility

    2026-02-24, 8:30 AM

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    Paul Larochelle
    Senior Director Global Clinical Supply Chain,
    Takeda

    Paul Larochelle currently serves as Senior Director (Planning Team Lead) for Global Clinical Supply Chain at Takeda, where he serves as a member of the GCSC Leadership Team and is responsible for managing a team of professionals overseeing the forecasting and planning of clinical study supplies. His role encompasses the strategic and operational aspects of clinical supply chain management in therapeutic areas such as oncology, neuroscience, gastrointestinal diseases, vaccines, and rare diseases. Paul's leadership extends to cross-functional projects aimed at implementing new capabilities, conducting due diligence of potential acquisitions by the company, and improving existing processes.

    Previously, Paul held various roles at Biogen Corporation and Genzyme, a Sanofi Company, where he honed his expertise in clinical asset planning and clinical supplies management. His contributions to these organizations included serving as a lead contact for multiple clinical programs, developing supply chain strategies, leading continuous improvement projects, and serving as Fellowship Coordinator and Student Preceptor for dozens of students.

    Paul has a BS in Biology from Providence College, PharmD from MCPHS Boston, and an MBA from Worcester Polytechnic Institute. He also completed a Post-PharmD Industry Fellowship in Clinical Research/Investigational Product Management with MCPHS-Worcester and Genzyme Corporation. He is Chair of the Dean's Advisory Board at MCPHS School of Pharmacy – Boston,  a member of the Pharmacy Advisory Board at Western New England University, and a member of the Advisory Board for the Clinical Trial Supply global conference series.

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    Ruth Atterbury

    CTS Portfolio Manager