Uncertainty is the only certainty in clinical trial supply chains. From shifting regulations to supply shortages and cybersecurity threats, one unexpected disruption can derail an entire trial. The key to success? A proactive, strategic approach to risk management.
The Top 8 Risk Management Strategies is an essential, action-driven checklist designed to help clinical trial supply professionals identify, assess, and mitigate risks across the entire supply chain.
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Risk management isn’t just about crisis response, it’s about proactive prevention and this infographic will help you stay compliant with global regulations, minimise supply chain disruptions, rnsure patient access to critical trial materials, and enhance resilience in an unpredictable global industry.
Sustainability is no longer a choice, it’s a necessity in clinical trial supply chains. With increasing regulations, growing environmental responsibilities, and the push for more efficient, patient-centric operations, it’s time to take action. The Sustainability Improvement To-Do List is your clear, step-by-step guide to integrating sustainability into every stage of your supply chain, with a regional breakdown of sustainability initiatives across the EU, UK, and US.
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Sustainability isn’t just about compliance, it’s about future-proofing your supply chain and this infographic gives you clear, practical steps to meet evolving sustainability regulations across regions, reduce environmental impact while increasing operational efficiency, and ensure a resilient, patient-focused supply chain.
The clinical trial supply landscape is more complex than ever, with regulatory changes, supply chain risks, and sustainability pressures which demand smarter, faster, and more efficient solutions. The key? Leveraging technology
The Top 10 Technologies Checklist is your ultimate guide to integrating cutting-edge digital tools for a seamless, risk-proof clinical trial supply chain.
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This infographic t is your go-to resource for digital integration in clinical trial supply chains. Whether tackling global compliance, mitigating supply risks, or enhancing operational efficiency, this guide shows you exactly how to harness the power of technology for success. 📥 Download Now & Transform Your Clinical Trial Supply Chain
The clinical trials landscape is evolving rapidly—driven by innovative technologies, shifting patient needs, and a strong push for global inclusion. In this exclusive interview, Steve Jacobs, President of Global BioPharm Solutions, LLC, explains how clinical trial supply chains are being reshaped by new challenges and opportunities. From the rise of AI and automation to the shift towards decentralised, patient-centric trials, Steve offers valuable insights on how the industry can not only adapt but thrive.
Discover how embracing cutting-edge technology, reinforcing data integrity, and championing sustainability will future-proof clinical operations in a complex, diverse world.
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The future of clinical trials is unfolding—join this transformative journey today!
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.
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Stay informed and prepared—download this fact sheet today to optimise your supply chain strategy in an increasingly complex regulatory environment.
The clinical trial supply chain is undergoing a radical transformation. With the complexity of multi-indication treatments and rare disease trials driving new challenges, innovative technologies and strategies are now essential. In this interview, Steve Jacobs, President of Global BioPharm Solutions, LLC, explains how advanced tools and patient-centric approaches are reshaping every link in the supply chain.
Steve discusses how AI, automation, and digital tools are streamlining operations—from accurate forecasting and data collection to efficient drug returns and reconciliation. These innovations not only boost efficiency and data quality but also help overcome challenges like supply kit expiries and comparator shortages. He also highlights the benefits of decentralised, direct-to-patient models that improve enrolment and retention while ensuring regulatory compliance and sustainability.
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Embrace the future of clinical trial supply management where cutting-edge technology meets smart, sustainable strategy.