25th Annual Clinical Trial Supply Europe 2024

2024 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.

6 - 7

March

2024
  • Hyatt Regency Barcelona Towers, Barcelona, Spain
  • Complimentary
  • Why attend?
  • Agenda
  • Speakers
  • Plan Your Visit
  • Sponsors
  • Media Centre
  • Contact Us
close

Featured Speakers

Back

Arnaud Dourlens​

Head of Clinical Trial Supply, 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.

Next speaker
Back

Giuseppe Coppola​

Head of Global Clinical Supply Operations, Novartis

Next speaker
Back

Claudio Semeraro​

Associate Director, Cell and Gene Therapy Lead, UCB

Next speaker
Back

Adam Pitt​

Biological Threat Exclusion Coordinator (BTEC), U.S. Customs and Border Protection

Adam Pitt is a Biological Threat Exclusion Coordinator (BTEC) for CBP in the Office of Field Operations/ Agriculture Programs and Trade Liaison/ Biological Threat Exclusion. As a BTEC, Mr. Pitt is charged with supporting and developing U.S. Customs and Border Protection (CBP) operational capacity and capability in preventing tools of agro/bio-terrorism from entering the U.S. Mr. Pitt has more than 18 years of public service with CBP and the National Institutes of Health (NIH), and has worked in a variety of environments, including air passenger, cargo, and express consignment carrier locations.

Next speaker
Back

Marcus Wajngarten​

Senior Director, Home Supply, AstraZeneca

Marcus has been realizing innovative solutions and clinical science in the Pharma space for almost 20 years.

Passionate in driving operational value with technology, the science and the patient is always in focus.

As part of AstraZeneca’s Digital Health transformation, he is aiming to bring greater value to patients faster though technology.

Marcus is gearing up AstraZeneca’s capabilities to take on De-centralized trials, with patient centricity at heart.

Next speaker
Back

Adam Pitt​

Biological Threat Exclusion Coordinator

Next speaker
Back

Niklas Mattsson​

Director, Comparator Management, MSD

At MSD from 2012 and before worked with comparator sourcing since 2004 at a few wholesalers and a CMO. Started career in product management of medical devices and OTC products. M.Sc. in Engineering in 1995 and proficient in English, German, Italian and Swedish.

Next speaker

    Sponsors Include:

    Back

    Company Information

    Simply sourcing comparators – we offer a unique blend of small company flexibility and speed, backed with the large-scale buying power of the Orifarm Group, which is one of the largest pharmaceutical suppliers in Europe. With over €1.4B products sold in 2021 and more than 4,000 unique product lines sourced on a monthly basis, we have unparalleled access to “out of market” and manufacturer direct buying capability, both in the US and Europe.

    Company website: www.Orifarm-CTS.com

    Company Website

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

    Next Sponsor
    Back

    Company Information

    Medidata is leading the digital transformation of life science, with the world’s most used platform for clinical development, commercial, and real-world data. Rave RTSM is the only fully pre-validated randomization and trial supply management solution that can be configured in minutes and enables mid-study changes with minimal downtime and no change orders. RTSM is built on Rave EDC, so there is no double data entry and minimal reconciliation expediting study start-up and study-close out. Rave RTSM streamlines your operations and provides real-time visibility for your study teams. https://www.medidata.com/en/clinical-trial-products/clinical-data-management/rtsm/

    Company Website

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

    Next Sponsor
    Back

    Company Information

    TecEx Medical is an Importer of Record (IOR) and customs compliance specialist in the international clinical trial sector. With a team of professionals dedicated to successful importation (or exportation) of clinical trial supplies, we work with Sponsors, CROs, CMOs and Vendors to manage the clinical trial lifecycle.

    Company Website

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

    Next Sponsor
    Back

    Company Information

    SanaClis was founded in 2000 by seasoned industry experts all of whom have had executive level positions in leading pharma companies and large global CROs. SanaClis is the Full service CRO that offers comprehensive range of services for clinical trials in Europe with focus in Central and Eastern Europe.

     

    Company Website

    To learn more , please visit our website - http://www.sanaclis.eu/

    Next Sponsor
    Back

    Company Website

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

    Next Sponsor
    Back

    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/

    Next Sponsor
    Back

    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/

    Next Sponsor
    Back

    Company Information

    At RxSource, our passion drives us to be the bridge between pharma and patient. With offices in Canada, USA and Ireland we provide bespoke global clinical trial supply management services to pharma, biotech and CROs. Whether it’s employing demand-led packaging, a local sourcing model or another flexible option, we guarantee on-time delivery without compromising quality. Our clients are our partners; success for them = success for us.

    Company Website

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

    Next Sponsor
    Back

    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/

    Next Sponsor
    Back

    Company Website

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

    Next Sponsor
    Back

    Company Information

    Since 1997, Clinigen has offered market-leading clinical trial supplies and biological sample management services to meet the most complex clinical supply challenges. Part of Clinigen Group’s global supply chain facility and depot network, we deliver tailored solutions for clients to ensure their clinical trials are a success, regardless of size or scope, from Phase I to Phase IV projects.

    Company Website

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

    Next Sponsor
    Back

    Company Information

    Bionical Emas is a global Contract Research Organization (CRO) combining Clinical Development, Clinical Trial Supply (CTS) and Early Access Programs (EAP) bringing life-changing medicines to patients around the world. Our Clinical Trial Supply Division has a global vendor network of manufacturers, wholesaler distributors and optimized sourcing strategies to support your study. Whether you require products locally sourced in emerging markets and distributed directly to trial sites, global sourcing of high-value commercial drug products, or a demand-driven sourcing approach, we have the right solution for you.

    Company Website

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

    Next Sponsor
    Back

    Company Website

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

    Next Sponsor
    Back

    Company Information

    Brocacef operates throughout the entire pharmaceutical chain, lending us an unique position as a wholesaler in the Dutch pharmaceutical healthcare industry. With expertise in global logistics, sourcing and supply chain experience Brocacef is able to offer a variety of services for clinical trials.

    Company Website

    To learn more , please visit our website - www.brocacef.nl

    Next Sponsor
    Back

    Company Information

    Abacus Medicine Pharma Services is the new name for the healthcare and pharma services company previously known as Aposave. The company has three service lines: Clinical Trial Solutions (CTS), Commercial Partnerships and Unlicensed Medicines.

    The CTS service focuses on comparator sourcing solutions for clinical trials as well as bespoke batch-specific sourcing of pre-clinical samples. We specialize in partnering biosimilar manufacturers, biotechnology and innovative pharma companies

    Company Website

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

    Next Sponsor
    Back

    Company Information

    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.

    Company Website

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

    Next Sponsor
    Back

    Company Information

    Pharma14 – Global medicine database platform.
    Covers 68 countries and deals in the tracking of finished dosage formulations as well as business analysis tools.
    Tracking all registered medicines, prices, consumption data, reimbursement data and more.
    Please stop by for a live demonstration and see how we can assist your company needs.

    Next Sponsor
    Back

    Company Information

    Cold Chain Technologies (CCT) is an industry recognized technical leader in the development and delivery of single-use and reusable insulated thermal packaging solutions that protect the integrity of temperature sensitive payloads. With over 50 years of experience in the global cold chain, we fully understand its’ logistics and applications, demands, and extremes. CCT is a pioneer in the design and delivery of innovative and high-quality thermal packaging, and one of the industry’s largest cold chain solution providers.

    CCT is a leading global provider of single-use and reusable thermal packaging solutions for the distribution and transport of temperature-sensitive shipments and are distributed from multiple U.S. and International locations that include Europe, Latin America, and Asia.

    Company Website

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

    Next Sponsor
    Back

    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/

    Next Sponsor
    Back

    Company Information

    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 41,160 employees in 108 locations in 53 countries as at June 30, 2023. For further information about ICON, visit: www.iconplc.com.

    Company Website

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

    Next Sponsor

      Why attend?

       

      2024 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.

      After the disruption to the global clinical supply chain over the past two years, attendees will once again be able to benefit from networking and learning in a safe, face-to-face environment. There’s never been a better time to exchange case studies, meet socially-distanced 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 2024?

      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

      • 6 Mar 2024
      • 7 Mar 2024
      Expand All

      Streams

      Stream one

      Clinical Supply Logistics and Operations

      Stream two

      Clinical Supply Technology and Innovation

      11 AM

      Increasing diversity: supply chain considerations for clinical trials in Africa

      • Navigating benefits and challenges: a deep dive into the diverse landscapes of African clinical trials, highlighting the unique opportunities and overcoming prevalent obstacles
      • Optimizing supply logistics: strategies for efficient and compliant shipment of trial supplies from Europe into Africa, with a focus on navigating the entry requirements and logistics networks
      • Regulatory navigation and compliance: an exploration of the regulatory environment across Africa's varied jurisdictions, ensuring trial supply compliance with local and international standards
      • Cultural competence in trial supply management: addressing the need for sensitive and appropriate packaging and labeling, including translations and adaptations, for clinical trials across different African cultures and languages

      Speakers

      11:30 AM

      Reserved for Suvoda

      12 PM

      Clinical supply chain performance ecosystem synergies

      • Tools
      • E2E supply
      • R&D goals

      Speakers

      12:30 PM

      Reserved for 4G Clinical

      1 PM

      Lunch and networking

      2 PM

      Case Study: Seizing the benefits of e-labelling in conjunction with user apps

      • Scanning barcodes or QR codes on e-labelling: benefits and challenges
      • Tracking patient data and GDPR considerations
      • Implementing and using e-labelling with patient apps

      2:30 PM

      Reserved for IQVIA

      \

      3 PM

      Understanding how a strategic partnership is essential to adapt to Gene Therapy paradigm shift of the entire supply chain

      • Reviewing strategic partnering model for gene therapy
      • Considering supply chain requirements specific to cell and gene therapy
      • Analysing how the partnership was key for successful implementation

      Speakers

      3:30 PM

      Afternoon refreshments, networking and prize draw

      4 PM

      Evolving use of automation, AI and machine learning in clinical trial supply chain to reduce costs and streamline processes

      • Identifying where and how data-driven technologies can be incorporated to streamline processes within clinical supply chains
      • Reviewing cost savings through use of AI and big data
      • Evaluating benefits of using blockchain technologies to enhance conduction and management of trials
      • Highlighting successes of implementing AI and machine learning tools through case study examples

      4:30 PM

      Reserved for TSS

      5 PM

      Panel Discussion: Leveraging technology to assist with increasingly complex supply chains

      • Simplifying processes via use of technology to reduce complexity challenges
      • Reviewing available technology and processes to assist with monitoring supply chain
      • Driving end to end supply chain digitalisation to improve visibility and data exchange
      • Leveraging digitalization in conjunction with quality requirements for complex supply chains – what we can learn from commercial supply

      Speakers

      7:30 AM

      Registration and refreshments

      8:15 AM

      Chairperson’s opening remarks

      Speakers

      8:30 AM

      Keynote: Focusing on sustainability in supply chain to improve ESG responsibilities and comply with upcoming regulations

      • Preparing for EU Corporate Sustainability Reporting Directive (CSRD)
      • Understanding how to measure carbon footprint
      • Considering quick wins to do now and focuses for future

      Speakers

      9 AM

      Reserved for Medidata

      9:30 AM

      Securing your global supply chain through designing an agile and resilient end to end supply chain that maximises adaptability

      • Designing an adaptable supply chain to remain agile in the face of disruptions
      • Improving quality processes to shorten supply chain lead times and drive agility
      • Leveraging technologies to improve your visibility and end to end supply chain

       

      Speakers

      10 AM

      Reserved for N-Side

      10:30 AM

      Morning refreshments and networking

      11 AM

      Fireside Chat: Effectively forecasting and organising pool supply to reduce wastage and increase sustainability

      • Working together to harness benefits and overcome challenges of pool supply
      • Using just in time labelling to increase flexibility of drug use
      • Reducing waste and improving sustainability

      Speakers

      11:30 AM

      Reserved for Berlinger

      12 PM

      Global shortages on a rise – urgent actions for sustainable CTS procurement needed

      • Highlighting challenges and impacts of global supply shortages
      • Realising urgent need to increase sustainability and life cycle of drug products to avoid limiting innovation due to shortages
      • Overcoming shortages to keep your trial on track

      Speakers

      12:30 PM

      Reserved for TecEx Medical

      1 PM

      Lunch and networking

      2 PM

      Transforming comparator sourcing models to improve supply optimization

      • Sharing contacts within clinical trial sales and comparator sourcing widely to enable easy access and direct negotiations
      • Outlining advantages for sponsors, manufacturers and wholesale suppliers
      • Uncovering case study examples and successes of new sourcing model

      Speakers

      2:30 PM

      Reserved for Abacus Medicine

      3 PM

      Working hand in hand with quality team to ensure compliance and reduce delays

      • Aligning early phase vs late phase quality assurance considerations with supply chain protocols to minimize disruptions and backlogs in supply chain
      • Understanding importance of role and responsibility of a Qualified Person and timelines required for QP release
      • Uncovering common QA compliance oversights and how to avoid them

      3:30 PM

      Afternoon refreshments, networking and prize draw

      4 PM

      State of the biopharma industry: the outlook for drugs, trials, and manufacturing

      • What’s coming in the pharma pipeline?
      • Drug manufacturing for clinical trials
      • Emerging trends: gene therapy, mRNA, and AI
      • Opportunities for contract development and manufacturing organisations (CDMOs)

      Speakers

      4:30 PM

      Reserved for Almac

      5 PM

      Panel Discussion: Selecting clinical trial supply vendors wisely and maintaining oversight to keep your trial on track

      • Vetting supply vendors, considering size and scale to ensure best fit
      • Considering how to maintain oversight of multiple vendors within one clinical trial study
      • Deciding how much oversight is right for each different vendor
      • Setting clear objectives and communicating effectively between sponsor and vendors to ensure the most efficient collaboration

      Speakers

      5:30 PM

      Chairperson’s closing remarks

      Speakers

      Streams

      Stream one

      Clinical Supply Logistics and Operations

      Stream two

      Clinical Supply Technology and Innovation

      9 AM

      Creating a successful direct to patient supply distribution strategy

      • Creating and implementing suitable strategies per study
      • Complying with regulatory frameworks
      • Optimising supply chain flexibility within direct to patient trials
      • Overcoming common challenges and pitfalls in direct to patient supply

      Speakers

      9:30 AM

      Reserved for Thermo Fisher Scientific

      10 AM

      Clinical supply chain responsibilities for study close out, end of trial and returns

      • Clinical Trial Master File and Data Base Lock
      • IRT compliance – expected reports, accountability logs, what auditors are looking for
      • How to prepare for closeout at study design to ensure reporting is maintained throughout
      • Pre-planning for supply destroys and returns to ensure compliance destroying onsite or nearby

      10:30 AM

      Reserved for event sponsor

      11 AM

      Morning refreshments and networking

      8 AM

      Registration and Refreshments

      8:55 AM

      Chairperson’s opening remarks

      Speakers

      9 AM

      Panel discussion: Preparing for and mitigating against risk in clinical supply chain to avoid delays

      • Creating a risk management plan for clinical supply chain
      • Considerations for security risk management
      • Preparing for unexpected and natural disasters
      • Monitoring temperature control risk management

      Speakers

      9:30 AM

      Reserved for Biocair

      Speakers

      10 AM

      Working closely with clinical departments to reduce supply impacts further down the line

      • Communicating early regarding patient recruitment; sites and countries for supply team logistics
      • Considering the size of the trial; amount of supply required to forecast and distribute
      • Understanding import, packaging and labelling regulations for multiple countries

      10:30 AM

      Reserved for event sponsor

      11 AM

      Morning refreshments and networking

      11:30 AM

      Navigating multiple regulatory agencies to help expedite supply chain times

      • Understanding the requirement and options for declaring biological materials to U.S. Customs and Border Protection (CBP)
      • Review of key U.S. regulatory agency authorities, such as CDC, FDA, USDA, and CBP
      • Discovering the latest non-compliant shipment issues for biological materials and pharma products and tips to avoid them
      • Learning about valuable resources and contacts for assistance

      Speakers

      12 PM

      Reserved for event sponsor

      12:30 PM

      Fireside Chat: Working with Uber Health transportation in clinical trials to improve equity and increase participant retention

      • Increasing socio demographic diversity in clinical trials by supplying to patients who can’t attend sites without assistance
      • Improving adherence to clinical trial participation by providing transportation for repeat appointments
      • Sharing case study examples and results

      Speakers

      1 PM

      Lunch, networking and prize draw

      2 PM

      PROBLEM-SOLVING ROUNDTABLE DISCUSSIONS

      During the roundtable discussion session, the conference hall will be divided into two ‘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 clinical trial supply. After 45 minutes, delegates will have the opportunity to swap and choose a different table, and each roundtable will run twice.

      ROUNDTABLE 1: Importing and exporting biological materials to or from the U.S

      Adam Pitt, Biological Threat Exclusion Coordinator, U.S. Customs and Border Protection
      George Amerson, Biological Threat Exclusion Coordinator, U.S. Customs and Border Protection

      ROUNDTABLE 2: Discussing impacts of CTIS on clinical supply teams

      ROUNDTABLE 3: Overcoming Import of record challenges in clinical supplies

       

      Speakers

      3:30 PM

      Chairperson’s closing remarks

      Speakers

      Speakers

      Select a speaker to learn more

      Back
      Niklas Mattsson
      Director, Comparator Management, MSD

      At MSD from 2012 and before worked with comparator sourcing since 2004 at a few wholesalers and a CMO. Started career in product management of medical devices and OTC products. M.Sc. in Engineering in 1995 and proficient in English, German, Italian and Swedish.

      Session Details:

      Transforming comparator sourcing models to improve supply optimization

      2024-03-06, 2:00 PM

      View In Agenda
      Next speaker
      Back
      Giuseppe Coppola
      Head of Global Clinical Supply Operations, Novartis

      Session Details:

      Panel Discussion: Selecting clinical trial supply vendors wisely and maintaining oversight to keep your trial on track

      2024-03-06, 5:00 PM

      View In Agenda
      Next speaker
      Back
      Arnaud Dourlens
      Head of Clinical Trial Supply, 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:

      Securing your global supply chain through designing an agile and resilient end to end supply chain that maximises adaptability

      2024-03-06, 9:30 AM

      View In Agenda
      Next speaker
      Back
      Dr 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:

      Panel discussion: Preparing for and mitigating against risk in clinical supply chain to avoid delays

      2024-03-07, 9:00 AM

      View In Agenda
      Next speaker
      Back
      Brendan Krause
      Head of International, Uber Health

      Brendan has over 20 years of policy, strategy and business development experience in health
      care. He began his career at the National Governors Association in Washington, DC, working
      on health reform between the US Federal Government and states. Following NGA, Brendan
      attended the London School of Economics as a Fulbright Scholar, where he studied the impact
      of the Blair Government's choice and competition reforms in the NHS and earned an MSc in
      International Health Policy and Economics. He then spent 12 years working for Optum in the
      UK in a number of UK and global strategy roles, with a focus on use of data to improve
      population health. Recently, Brendan joined Uber as Head of International for Health, where he
      is building a global strategy to remove transportation and logistics as a barrier to care.

      Session Details:

      Fireside Chat: Working with Uber Health transportation in clinical trials to improve equity and increase participant retention

      2024-03-07, 12:30 PM

      View In Agenda
      Next speaker
      Back
      Luiz Barberini
      Head of External Manufacturing, Latin America, Bayer

      Session Details:

      Panel discussion: Preparing for and mitigating against risk in clinical supply chain to avoid delays

      2024-03-07, 9:00 AM

      View In Agenda
      Next speaker
      Back
      Thomas Thoma
      Head Managed Access Programs, CTS/GHT/SR, Teva Pharmaceuticals

      Three University degrees at the University of Augsburg 5 years of Supply Chain Management responsibilities in automotive electronics industry 12 years of Management responsibilities in multiple roles (SCM, IT, Sales) in the pharma industry Since 2014 Head of Clinical Trial Supply (Sales) of Teva Europe. Offering Teva widest pipeline of pharmaceuticals, placebos and manufacturing for clinical trial purposes. Since 2017 Head of Global Health Tendering of Teva Global. Offering Teva widest pipeline to NGOs, GOs and UN related organizations. Married and father of three beautiful kids

      Session Details:

      Global shortages on a rise – urgent actions for sustainable CTS procurement needed

      2024-03-06, 12:00 PM

      View In Agenda
      Next speaker
      Back
      Mattia Scarafoni
      Senior Manager Global Clinical Supply Chain, Incyte

      Session Details:

      Fireside Chat: Effectively forecasting and organising pool supply to reduce wastage and increase sustainability

      2024-03-06, 11:00 AM

      View In Agenda
      Next speaker
      Back
      Jürgen Wieland
      Development Environmental Sustainability Lead, Novartis

      Session Details:

      Keynote: Focusing on sustainability in supply chain to improve ESG responsibilities and comply with upcoming regulations

      2024-03-06, 8:30 AM

      View In Agenda
      Next speaker
      Back
      Landry Giardina
      Global Head of Clinical Supply Chain Operations Innovation and Technology, Sanofi

      20y experience within pharmaceutical industry and specially within clinical supply chain & digital development.

      Knowledge acquired via several jobs such as vaccine supply manager, unit head of alignment supply (Drug product/marketed product) and more recently as Digital supply chain leader.

      Technology, innovation and data & team management are the main drivers of Landry’s career.

      Session Details:

      Clinical supply chain performance ecosystem synergies

      2024-03-06, 12:00 PM

      View In Agenda
      Next speaker
      Back
      Claudio Semeraro
      Associate Director, Cell and Gene Therapy Lead, UCB

      Session Details:

      Understanding how a strategic partnership is essential to adapt to Gene Therapy paradigm shift of the entire supply chain

      2024-03-06, 3:00 PM

      View In Agenda
      Next speaker
      Back
      Pierre-Gaultier Delheid
      Head of Clinical Vendor Management, UCB Pharma

      As Head of Clinical Vendor Management at UCB, Pierre-Gaultier Delheid leads the vendor strategy aiming to design and manage a strong external vendor network. He makes a point of honor to build sustainable and strong alliances to overcome clinical challenges in a flexibility, agile, reliable, green and cost-efficient way. In close collaboration with other UCB business units, he drives a culture of partnership to change the game to a better outcome.

      Engineer by background, his experience in bio-pharma industry in CDMO as well as in Sponsor companies and his business DNA gained during an international EMBA (Hult, US/UK) led him to build strong expertise in the field of operation and business optimization as well as building strong partnerships.

      Session Details:

      Understanding how a strategic partnership is essential to adapt to Gene Therapy paradigm shift of the entire supply chain

      2024-03-06, 3:00 PM

      View In Agenda
      Next speaker
      Back
      Ingrid Lux
      Head of Quality Disposition, Director, Oncology and External Supply Small Molecule EU, Takeda

      NULL

      Session Details:

      Panel Discussion: Leveraging technology to assist with increasingly complex supply chains

      2024-03-06, 5:00 PM

      View In Agenda
      Next speaker
      Back
      Fiona Barry
      Editor in Chief & Director Pharmsource, GlobalData

      Session Details:

      Chairperson’s opening remarks

      2024-03-06, 8:15 AM

      Session Details:

      State of the biopharma industry: the outlook for drugs, trials, and manufacturing

      2024-03-06, 4:00 PM

      Session Details:

      Chairperson’s closing remarks

      2024-03-07, 3:30 PM

      Session Details:

      Chairperson’s opening remarks

      2024-03-07, 8:55 AM

      View In Agenda
      Next speaker
      Back
      Adam Pitt
      Biological Threat Exclusion Coordinator (BTEC), U.S. Customs and Border Protection

      Adam Pitt is a Biological Threat Exclusion Coordinator (BTEC) for CBP in the Office of Field Operations/ Agriculture Programs and Trade Liaison/ Biological Threat Exclusion. As a BTEC, Mr. Pitt is charged with supporting and developing U.S. Customs and Border Protection (CBP) operational capacity and capability in preventing tools of agro/bio-terrorism from entering the U.S. Mr. Pitt has more than 18 years of public service with CBP and the National Institutes of Health (NIH), and has worked in a variety of environments, including air passenger, cargo, and express consignment carrier locations.

      Session Details:

      PROBLEM-SOLVING ROUNDTABLE DISCUSSIONS

      2024-03-07, 2:00 PM

      Session Details:

      Navigating multiple regulatory agencies to help expedite supply chain times

      2024-03-07, 11:30 AM

      View In Agenda
      Next speaker
      Back
      George Amerson
      Biological Threat Exclusion Coordinator, U.S. Customs And Border Protection

      George Amerson is a Biological Threat Exclusion Coordinator (BTEC) for CBP in the Office of Field Operations/ Agriculture Programs and Trade Liaison/ Biological Threat Exclusion. As a BTEC, Mr. Amerson is charged with supporting and developing U.S. Customs and Border Protection (CBP) operational capacity and capability in preventing tools of agro/bio-terrorism from entering the U.S. Mr. Amerson has more than 16 years of public service with CBP and has worked in a variety of environments, including air passenger, maritime, cargo and CBP Training Academy.

      Session Details:

      PROBLEM-SOLVING ROUNDTABLE DISCUSSIONS

      2024-03-07, 2:00 PM

      Session Details:

      Navigating multiple regulatory agencies to help expedite supply chain times

      2024-03-07, 11:30 AM

      View In Agenda
      Next speaker
      Back
      Révérien Uwacu
      Clinical Trial Supply Management Consultant, UCB

      Originally from Rwanda but studied and living in Belgium, Reverien has an IT and Supply Chain academic background. Professionally, he is a pharma Supply Chain Consultant with 12+years’ experience. Reverien’s experience includes companies such as Johnson and Johnson, UCB, Baxter, and Thermofisher.

      Session Details:

      Increasing diversity: supply chain considerations for clinical trials in Africa

      2024-03-06, 11:00 AM

      View In Agenda
      Next speaker
      Back
      Marcus Wajngarten
      Senior Director, Home Supply, AstraZeneca

      Marcus has been realizing innovative solutions and clinical science in the Pharma space for almost 20 years.

      Passionate in driving operational value with technology, the science and the patient is always in focus.

      As part of AstraZeneca’s Digital Health transformation, he is aiming to bring greater value to patients faster though technology.

      Marcus is gearing up AstraZeneca’s capabilities to take on De-centralized trials, with patient centricity at heart.

      Session Details:

      Creating a successful direct to patient supply distribution strategy

      2024-03-07, 9:00 AM

      View In Agenda
      Next speaker

      Plan Your Visit

      Hyatt Regency Barcelona Towers

      Avinguda de la Granvia de l’Hospitalet, 144, 08907 Barcelona, Spain

      Sponsors

      Select a sponsor to learn more

      Featured Sponsors

      Session Sponsors

      Exhibitors

      Media Centre

      MEDIA PARTNERS

      Become A Media Partner

      WHAT TO EXPECT FOR 2023?

       

      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.

      See What It's All About

      Enquiry

      Contact Us

      SPONSORSHIP ENQUIRIES

      Jaz Sidhu

      Senior Sponsorship Manager

      +44 (0) 20 7947 2755

      SPEAKING OPPORTUNITIES

      Ruth Atterbury

      Portfolio Manager

      +44 (0) 204 540 7766

      MARKETING ENQUIRIES

      Moona Popal

      Marketing Manager

      DELEGATE ENQUIRIES

      Sunny Saikia

      VIP Delegate Manager

      SPONSORSHIP ENQUIRIES

      To enquire about sponsorship opportunities for the conference, please contact:

      Jaz Sidhu

      Senior Sponsorship Manager


      +44 (0) 20 7947 2755

      SPEAKER ENQUIRIES

      To enquire about speaking opportunities for the conference, please contact:

      Ruth Atterbury

      Portfolio Manager


      +44 (0) 204 540 7766