Clinical trial supply chains are evolving rapidly, and with them, the need for smarter, patient-centric solutions has never been clearer. That's why our Clinical Trial Supply Forum 2025 is dedicated to tackling today's pressing supply chain challenges while equipping you with the tools to succeed in the trials of tomorrow. We've crafted this forum with input from leading clinical trial supply experts across the pharmaceutical landscape-large and small companies, CROs, and innovative solution providers.
LEAN. GLOBAL. END TO END.
75+ Hours Researching with Industry
100+ Attendees
20+ Speakers
2 Workshops
10 Hours of Networking Opportunities
In planning the 2025 Clinical Trial Supply Forum, we engaged with a number of clinical trial supply experts from across the pharmaceutical spectrum-spanning large and small companies, CROs, and solution providers. They all shared a clear message: modern clinical trials demand a smarter, more patient-centric supply chain, where adaptability, sustainability, and advanced planning are the cornerstones of success.
To meet these evolving challenges, the Clinical Trial Supply Forum 2025 will take a deep dive into the pressing gaps in today's supply chains. The conference will offer actionable insights and cutting-edge solutions for building a more agile, technology-driven, and sustainable framework. Through interactive workshops, in-depth panel discussions, and real-world case studies, attendees will leave equipped to tackle the complexities of trial supplies with confidence.
Our 2025 forum will empower you to:
Plan smarter with a holistic view of the supply chain
Build resilience against disruptions through better risk management
Drive patient-centred outcomes while embracing sustainability
Join us this May as we pave the way toward smarter trial supplies - ensuring that every stage, from lab to living room, is optimized for the trials of tomorrow.
Let's shape the future of clinical trial supplies together!
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.
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 Sustainable Supply Chains
Harness 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
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
Speakers
Kamal Amin, Head of Supply Management, Galderma
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
Cut Off Date: Please book your rooms before 11th April 2025 to receive the discounted rate. After this date all bedrooms are subject to availability and rate at the time of booking.
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.
