Clinical Trial Supply Conference 2026

Creating Smarter, Greener and Faster Clinical Trial Supply Chains

May 12-13, 2026 - Amsterdam, Netherlands

Manage Supply Chain Risks With Smarter, Greener And Faster Clinical Supplies

An effective clinical trial supply chain ensures the right product reaches the right patient, in the right quantity, at the right time. Enabling trials to run smoothly, ethically, and efficiently. The global clinical trial supplies market is set to reach $8.18 billion by 2030, growing at 8.9% annually. This growth is driven by rising pharmaceutical and biotech R&D investment, expanding drug pipelines, the prevalence of complex diseases, and the shift towards decentralised and adaptive trial designs.

However, despite the impressive growth, the clinical trial supply chain faces ongoing challenges: inaccurate demand forecasting, complex global distribution, temperature-sensitive logistics, and limited real-time visibility. These issues are fuelling the need for smarter, faster, and greener supply chains.

We have listened to these concerns and are proud to present the Clinical Trial Supply Forum, designed to tackle clinical trial supply chain challenges head-on. The conference features dedicated streams covering risk management, logistics, packaging, labelling, and storage, providing actionable insights to make every part of the supply chain smarter, greener and faster.

Why Attend Clinical Trial Supply 2026?

  • A Sharper Focus on Smarter, Faster, Greener Supply Chains: Dive deeper into how organisations can optimise every step of the supply chain - from packaging and labelling innovation to storage solutions, logistics efficiency, and sustainability strategies.
  • Open-Access Workshops: Practical workshops, open to all, will provide hands-on insights, real-world case studies, and opportunities to engage directly with specialists.
  • A Re-imagined Event Format: This year introduces a streamed programme designed to deliver a more cohesive narrative around the end-to-end clinical trial supply chain. Follow curated content streams tailored to your role, priorities, and levels of expertise.
  • More Meaningful Networking: The event will feature intimate peer-to-peer networking opportunities, designed to encourage open dialogue, problem-solving and relationship-building in smaller, high-value groups.

Peer-to-Peer Learning and Networking Guaranteed With:

  • 75+ Hours researching with industry
  • 100+ Attendees
  • 20+ Speakers
  • 2 Workshops
  • 10 Hours of networking opportunities

Key Focus Areas Include:

  • Strategic Planning: Optimizing supply chain operations to anticipate and adapt to trial complexities and patient needs.
  • Technology Powering Clinical Trial Supply: IRT & RTSM: Leveraging digital tools and data analytics to streamline processes, improve forecasting, and enhance end-to-end visibility.
  • Environmentally Sustainability: Advancing green practices that reduce the carbon footprint of clinical supplies while maintaining compliance and reliability.
  • Evolving Regulations - Discussing GMP &GDP: Explore practical approaches to regulatory compliance as regulatory expectations evolve in response to decentralised and adaptive trials, with greater focus on temperature control and end-to-end traceability.
  • Advanced Therapies: Explore the impact of advanced therapies on building future-ready clinical trial supply chains, including the unique requirements of cell and gene therapies, personalised medicines, and other complex, high-value treatments.
  • Sign up today!: Join us to shape the next generation of clinical trial supplies, one that’s equipped to handle the complexities of tomorrow’s clinical landscape while maintaining a strong commitment to patient care, innovation, and environmental responsibility.

Transform Your CTS Chain: Smarter, Faster, Greener Clinical Supply Strategies

  • Build A Smarter CTS Chain: Explore How to Optimise Forecasting, Enhance Inventory Visibility, and Leverage Data-Driven Planning to Reduce Waste and Costs.
  • Develop A Faster CTS Chain: Learn How to Improve Distribution Efficiency, Accelerate Time-to-Patient, and Streamline Global Operations for Complex Trials.
  • Create A Greener CTS Chain: Discover Strategies to Implement Sustainable Packaging, Reduce Carbon Footprint, and Adopt Greener Transport and Storage Solutions


The forum was very effective. Good for information exchange and networking. Well organised event too with clear instructions and good balance of breaks for networking.

Sr Manager- Global Logistics, Celgene

Very valuable to get an insight what other companies are planning, what challenges they have and discuss possible solutions

Senior Manager Clinical Supply Optimization Servcies CH & Asia, ThermoFisher

Great value event, enjoyed networking and the latest thinking from like minded professionals

Director, Clinical Supply Systems, Janssen

Round table discussions and networking was valuable. Very interesting talks and in discussions throughout the two days

Senior Supply Chain Specialist, Novo Nordisk

2026 Speaker Faculty

  • Wil Cools – Clinical Supply Leader, Galapagos
  • Raffaella Fallone – Clinical Data Management & Clinical Supply Lead, Angelini Pharma
  • Alessandro Amato – Clinical Supply Support, Angelini Pharma
  • Catherine Crespin – Clinical Labelling & Packaging Supply Lead, UCB
  • Audrey Aubert – Clinical Supply Compliance Process & Governance Lead, UCB
  • Chiara Venuti – Member of the Management Board, Cool Chain Association
  • Michelle Devine – Clinical Trial Supplies Management, LEO Pharma
  • Jennifer Lees – Patient Advocate, Sharing Harlyn’s Story
  • Puvi Bala – Director, Clinical Trial Services, Novitan
  • Lana Morrison – Clinical Supplies Manager, Summit Therapeutics
  • Vanessa Buonavoglia – Master Data Operations Lead, UCB Clinical Trial Supply Chain
  • Allyson De Meulder – Head of Internal Clinical Supply Quality, UCB
  • Taleb Tayeh – Senior Clinical Trial Supplies Manager, Debiopharm
  • Svetlana Soshko – IRT Maintenance Coordinator, Novo Nordisk
  • Kamal Amin – Head of Supply Management, Galderma
  • Samantha Carmichael – Lead Pharmacist, Clinical Trials, NHS Greater Glasgow and Clyde
  • Nelly Conus – Head of Medical Research, Cardiology Study Team, Insel Gruppe
  • Niklas Mattson – Director, Comparator Management, MSD
  • Claudio Semeraro – Director, Head of Candidates and Assets Supply, UCB
  • Henk Dieteren – Clinical Supply Chain Solutions Consultant, Suvoda
  • Steven Jacobs – President, Global BioPharm Solutions, LLC
  • Karen Crooks – Associate Director, Clinical Supply Chain, IO Biotech
  • Peter Sas – Associate Director, Compliance & Continuous Improvement, Johnson & Johnson
  • Kimi Le – Head of Clinical Trial Supply, Immunic Therapeutics
  • Miguel Silva – Clinical Trials Supply Chain Manager, Eli Lilly & Company
  • Stephanie Fitt – Head of European Sales, EMBALL’ISO

Please fill in your name and email to receive the Conference Agenda of this event.

Venue

Novotel Amsterdam City
Europaboulevard 10, 1083 AD
Amsterdam Netherlands

+31 20 721 9179

Group Rate: We have a discounted bedroom block available to our conference attendees with a rate of €189 including breakfast & VAT but excluding 12.5% city tax.

Reservation Method: Reserve your room by clicking on this link.

Please note: We will never recommend, approve or appoint any third party rooming service to act on our behalf. Please be extremely wary if you are approached by any such companies. We will always endeavour to negotiate the best available rates for you so please use the link provided above; this shows live availability and rates for all hotels in the area and allows you to book directly with the hotel of your choice within your budget.
Event details
Organizer :IQEU
Event type :Conference
Attendance :Physical Event
Reference :ASDE-25934