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The Clinical Trial Supply Forum 2025 Agenda

The Clinical Trial Supply Forum 2025 Agenda

The Clinical Trial Supply Forum (13-15 May, 2025 in Brussels, Belgium) is a platform where Clinical Trial Supply professionals on all seniority levels gather to exchange exclusive insights, establish valuable connections and collaboratively tackle industry challenges.

Join your peers in discussions around: 

  • Patient experiences and their relationship to clinical trial supplies
  • Direct-to-patient & Advanced direct-to-patient
  • From bench to bedside - gene therapy focus
  • Supply Chain Management - Supply chain toolkit and RTSM data integration
  • Data Management - Importer of records
  • Future Trends - What will clinical trial supply chain look like in ten years?

Download the agenda to view the full speaker line-up, and learn more about the workshops, panel debates, keynote presentations and more that will take place across the three event days >>

Infographic: A Step-by-Step Guide to Building a Clinical Trial Supply Strategy

Infographic: A Step-by-Step Guide to Building a Clinical Trial Supply Strategy

In an era where clinical trials are becoming increasingly complex and global, developing a robust supply strategy is more critical than ever. This strategic framework is designed to help you navigate the complex landscape of clinical trial supply, offering a step-by-step approach to crafting a resilient and adaptable strategy.

Clinical Trial Supply Forum 2024 Trends Report

Clinical Trial Supply Forum 2024 Trends Report

The clinical trial supply industry is going through a period of rapid change, propelled by the aftermath of the pandemic and the rapid evolution of technology. Additionally, world-changing geopolitical events continue to impact supply chains across all sectors. Pharma IQ interviewed Advisory Board member and Event Chairman, Steven Jacobs, President of Global BioPharm Solutions LLC, and we are pleased to take this opportunity to share with you our annual review of the trends and complexities that are shaping and driving transformation across the -end-to-end clinical trial supply chain.

Download the Report to Uncover:

• Expert Analysis on Industry Evolution: Gain invaluable insights into the profound transformation of the clinical trial supply landscape, emphasising the shift towards proactive, strategic supply chain models and the integration of cutting-edge technologies like AI and IoT.

• Impact of Global Challenges on Supply Chains: Learn how recent geopolitical events and the aftermath of the pandemic have driven innovation, emphasising the need for resilience and agility in overcoming supply chain disruptions.

• Technological Advancements in Supply Management: Explore the role of digital transformation in revolutionising supply chain management, with a focus on automation, predictive analytics, and real-time decision-making to ensure the success and integrity of clinical trials.

• Sustainability and Efficiency as Core Priorities: Delve into the growing emphasis on eco-friendly logistics and the optimisation of resource use, highlighting sustainable practices and efficiency improvements as key drivers of future industry success.

Fact Sheet |  Staying Compliant in Complexity: A Guide to Clinical Trial Supply Regulations

Fact Sheet | Staying Compliant in Complexity: A Guide to Clinical Trial Supply Regulations

Navigating the evolving landscape of clinical trial supply chain regulations is a continuous challenge for pharmaceutical companies, CROs, and solution providers. With shifting compliance requirements across the EU, UK, and US, staying ahead of regulatory updates is essential for seamless trial execution and patient safety.

This Fact Sheet breaks down the complexities of global clinical trial supply regulations, providing actionable insights to help CTS professionals mitigate risks, ensure compliance, and build resilient, patient-centric supply chains and includes expert insights from Kamal Amin, Head of Supply Management, Galderma and Steven Jacobs, President, Global BioPharm Solutions, LLC.

Download to learn more about:

  • Regulatory Updates & Compliance: Understanding the latest changes in GDP, GMP, EU CTR, ICH E6 (R3), MDR, post-Brexit UK regulations, and FDA guidelines.
  • Risk Mitigation Strategies: Identifying potential regulatory risks and implementing proactive compliance measures.
  • Supply Chain Resilience: Developing strategies to enhance flexibility and stability in an evolving regulatory environment.
  • Sustainability in Clinical Supply: Exploring global initiatives to integrate sustainability into supply chain operations.
  • Patient-Centric Supply Chains: Ensuring timely and compliant delivery of trial materials to improve patient outcomes.

Stay informed and prepared—download this fact sheet today to optimise your supply chain strategy in an increasingly complex regulatory environment.

Post-Show Review: Top 10 Takeaways from the Clinical Trial Supply Forum: Infographic

Post-Show Review: Top 10 Takeaways from the Clinical Trial Supply Forum: Infographic

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.