Clinical Trial Supply Forum

13-15 May | Brussels, Belgium

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With 80% of trials falling short of initial enrolment targets and timelines, the clinical trial supply chain is at a critical turning point.

As personalized medicine and increasingly complex trial designs redefine the pharmaceutical landscape, the need for a more agile, patient-centered, and globally integrated supply chain has never been more urgent. Today’s challenges—including fragmented planning, technology gaps, sustainability concerns, and diverse site requirements—call for innovative, forward-thinking supply chain strategies.

Pharma IQ’s Clinical Trial Supply Forum offers an essential platform for addressing inefficiencies in clinical trial supply. By bringing together industry leaders, we will explore actionable strategies to modernize the supply chain, ensuring that it can meet the demands of today’s trials and adapt to those of tomorrow. Our goal is to collaboratively develop solutions that emphasize quality, speed, adaptability, and patient-centric care, all while maintaining a strong commitment to sustainability and regulatory adherence.

Key Focus Areas Include:

Strategic Planning: Optimizing supply chain operations to anticipate and adapt to trial complexities and patient needs.
The Role of Technology: Leveraging digital tools and data analytics to streamline processes, improve forecasting, and enhance end-to-end visibility.
Environmental Sustainability: Advancing green practices that reduce the carbon footprint of clinical supplies while maintaining compliance and reliability.
Patient-Centric Approaches & Diversity: Crafting supply strategies that put patients first, respecting diversity and unique site experiences to improve trial accessibility and outcomes.
Globalization & Collaboration: Developing frameworks that enhance coordination across borders and cultures, ensuring supply consistency and regulatory adherence worldwide.

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.

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What Attendees Will Takeaway From CTS 2025

Discover How To Build The Clinical Trial Supply Chain Today's Patients & Products Need & Demand

Investigate The Latest Approaches To Successfully Executing Decentralised & Direct-to-Patient Clinical Trials

Harness New Automation & AI To Unlock The Potential of Clinical Trial Supply Teams

Streamline Operational & Logistical Processes By Leveraging Technological Innovation Across the Clinical Trial Supply Lifecyle

Navigate An Increasingly Complex Regulatory Landscape By Exploring Practical Approaches To Regulatory Compliance

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Our 2025 Expert Speaker Panel Includes

Kamal Amin

Head of Supply Management

Galderma

Ana-Zeralda Canals Hamann

Senior Clinical Trial Supplies Manager

Debiopharm

Samantha Carmichael

Lead Pharmacist Clinical Trials

NHS Greater Glasgow and Clyde

Alexandra Tsioni

Associate Director, Clinical Supply Chain

TEVA

Nelly Conus

Digital and DCT Solutions Manager

Syneos Health

Claudio Semeraro

Director, Head of Candidates and Assets Supply

UCB

Thomas Thoma

Head Managed Access Programs- Clinical Trials, Global Health Tendering and UEUM

Mepha / Teva Switzerland

Révérien Uwacu

Clinical Trial Supply Freelance

UCB

Steven Jacobs

President

Global BioPharm Solutions, LLC

Karen Crooks

Associate Director, Clinical Supply Chain

IO Biotech

Ingrid Debruyne

Associate Director, Logistics Strategic Capabilities

Johnson & Johnson

Piotr Grzonkowski

Associate Director Clinical Supply Programme

AstraZeneca

Peter Sas

Associate Director Compliance & Continuous Improvement

Johnson & Johnson

Katriona Brooksbank

Innovation Lead

R&I Innovation Lead, NHS GGC Hon. Senior Lecturer, School of Cardiovascular & Metabolic Health, University of Glasgow

Kristel Rens

Director, Business transformation and Innovation

J&J

Davide Carluccio

Principal Global Clinical Operations Manager

Almirall

Alexandru Popa

Associate Director | Blockchain for Digital Supply Chain

MSD

Loris Sainlez

Performance & Systems Lead (Clinical Trials Supply Chain)

UCB

Camillo Rossi

Associate Director Clinical Trial Distribution

Eli Lilly & Company

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Convince Your Boss Letter

Present your boss with this customizable letter detailing the reasons why you should attend Clinical Trial Supply Forum 2024 from 14 – 16 May, 2024 in Brussels, Belgium. Just download the letter template below, adjust as necessary (or edit as needed) and submit! We hope to welcome you there!

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Clinical Trial Supply Forum 2024 Sample Attendee List

Interested in seeing who you may meet at Clinical Trial Supply Forum 2024? Download our sample attendee list to to find out

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Clinical Trial Supply Forum 2024 Trends Report

We sat down with Steven Jacobs, President of Global BioPharm Solutions LLC to explore key trends and complexities shaping the clinical trial supply chain landscape.

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Top 10 Takeaways from the 2023 Clinical Trial Supply Forum

Discover the key highlights and learnings from the 2023 Clinical Trial Supply Forum in a concise, informative infographic format and understand what's shaping the future of the clinical trial supply industry.

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Attendee Testimonials

"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."

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

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

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

"Absolutely interesting and engaging"

"Very valuable, the workshops were useful and made good connections"

"The open atmosphere between the attendees is extremely helpful to learn from each other's experiences in the identification of efficient solutions "

"This event was a great learning opportunity for me. I think that it speaks volumes regarding the collaborative nature of the event, when someone like me (attending my first conference, with only 3.5 years' experience in CTS) felt comfortable enough to ask questions and participate in the discussions. "