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

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: Identify potential regulatory risks and implement 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.