Clinical Supply Regulatory Videos

  1. Cell & Gene Therapy Supply Chain Challenges: Global, Integrated Solutions

    Industry experts share insights to help you mitigate supply chain risk and accelerate access to novel cell and gene therapies.

  2. The Catalyst Of Decentralized Clinical Trials: Combining Clinical And Digital 7/27/2022

    Decentralized clinical trials are made up of a multitude of elements, from in home clinical capabilities, logistics, digital platforms, and technology, to global reach and more. This webinar shares important factors to consider to build your DCT ‘molecule’ successfully.

  3. Clinical Supply Chain Strategies For Building Resilience

    Achieving supply chain resilience is crucial, and flexible distribution strategies and ready-to-use depot and logistics networks are instrumental in establishing limitless flexibility and expertise capable of identifying possible risks.

  4. Global Advantage With Free Trade Zones In China 7/14/2022

    Understand how free trade zones work, and explore a flexible and cost efficient way to supply clinical trials in China and around the globe.

  5. Smart Packaging In Clinical Trials: What Clinical Supply Teams Need To Know

    Clinical supply innovators from across the industry share their experiences and lessons learned as they work to normalize the use of adherence measurement tools and smart medicine packages.

  6. Navigating Regulatory Direct-To-Patient Considerations 5/20/2022

    This webinar aims to introduce the main regulatory themes, as well as provide a practical insight into converting regulatory theory to practical steps to enable DtP on global studies. 

  7. Impact Of Supplier Choice On APAC Clinical Trial Execution

    Choosing the right clinical packaging and supply chain partner to support APAC studies can vary significantly based upon which countries are involved and the types of services required.

  8. Key Considerations When Developing Your Combination Product 2/20/2024

    Succeed in combination product development by understanding the risk factors that may arise and implementing mitigation strategies that will streamline the device development process.

  9. Integrating Early Development With Clinical Supply

    In the era of seamless development, reducing time to the clinic and getting rapid approval is key. An integrated approach can accelerate timelines, avoid communication pitfalls, and improve outcomes.