Proactive Strategies to Evaluate & Mitigate Clinical Supply Risk
Summary:
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 session will also explore packaging and clinical supply chain services for global clinical trials with a specific focus on the Asia-Pacific (APAC) region.