Proactive Strategies To Evaluate And Mitigate Risk In The Clinical Supply Chain

Successful clinical trials are crucial for advancing a novel therapeutic to market and maintaining a competitive edge. However, clinical trials face risks such as supply shortages which can cause costly delays and impact the safety and well-being of the patients involved in the trial.

Learn about strategies that can help build an understanding of risk assessment when developing a clinical supply plan, in addition to how a study’s protocol requirements, drug characteristics, packaging specifications, and patient compliance concerns must be identified and addressed in order to mitigate risk to help achieve successful clinical supply outcomes. This webinar also explores packaging and clinical supply chain services for global clinical trials with a specific focus on the Asia-Pacific (APAC) region.