Drug Safety, Pharmacovigilance, and Risk Management

This session will cover the importance of drug safety, pharmacovigilance, and risk management throughout the clinical trial process. Topics will include strategies for detecting, assessing, and reporting adverse events, as well as best practices for risk communication and management. Discussions will explore the role of digital tools in improving safety monitoring and the impact of regulatory requirements on pharmacovigilance practices. Case studies will provide insights into effective risk management strategies.
 

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