Learn how to enhance the effectiveness of safety risk communication in light of evolving regulatory expectations.

Explore the basics of drug safety and safety sciences in this seven module eLearning bundle.

Review the strategic and operational aspects of global risk management including key concepts, principles, and tools necessary to develop risk management programs.

Review how to design, develop, and manage a quality system related to your pharmacovigilance system to achieve quality and regulatory compliance.

Analyzing and interpreting safety data throughout product development.

Learn how organizations structure their efforts and utilize their resources to improve the odds of successful development in this six module program.

Review the key benefits-risk assessment methods and how to incorporate the patient perspective.

Learn how to effectively plan, write, and communicate key safety information in pharmacovigilance documents while collaborating with safety professionals to ensure clear and impactful regulatory reporting.