12-13 May | Novotel Amsterdam City, Amsterdam
Welcome to the 16th Annual Clinical Trial Supply Forum!
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.
Pharma IQ has listened to these concerns and is 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.
Our 2026 Expert Speaker Panel Includes
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
Sharing Harlyn's Story
Patient Advocate
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
Sr. Clinical Trial Supplies Manager
Debiopharm
Samantha Carmichael
Lead Pharmacist Clinical Trials
NHS Greater Glasgow and Clyde
Miguel Silva
Clinical Trials Supply Chain Manager
Eli Lilly & Company
Kimi Le
Head of Clinical Trial Supply
Immunic Therapeutics
Peter Sas
Associate Director Compliance & Continuous Improvement
Johnson & Johnson
Karen Crooks
Associate Director, Clinical Supply Chain
IO Biotech
Steven Jacobs
President
Global BioPharm Solutions, LLC
Henk Dieteren
Clinical Supply Chain Solutions Consultant
Suvoda
Claudio Semeraro
Director, Head of Candidates and Assets Supply
UCB
Niklas Mattson
Director Comparator Management
MSD
Nelly Conus
Head of Medical Research, Cardiology Study Team
Insel Gruppe
Kamal Amin
Head of Supply Management
Galderma
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.
Attendee Testimonials
We look forward to welcoming you there!
Contact Us
To secure a seat, book online now. Or, for any assistance, please contact us below as a potential attendee or sponsor.
In Partnership With:
QUESTIONS?
Address: IQPC Ltd, 129 Wilton Road,
London SW1V 1JZ
Telephone: +44 (0) 113 210 042
Fax: 44 (0) 207 368 9301
Email: enquire@iqpc.co.uk
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