Drug safety is a primary concern throughout the medical product development lifecycle. This eLearning program provides the knowledge you need, from regulations and requirements through pre-market review and post-market monitoring. The comprehensive program includes six self-paced modules that have been designed using the latest instructional strategies to improve retention and make learning convenient for busy professionals.

Drug Safety eLearning Program | Online, Anytime

• Introduction to Drug Safety
• Drug Safety Regulatory Requirements
• Pre-Marketing Clinical Trial Safety
• Post-Marketing Safety Management
• Basics of Signal Detection and Pharmacoepidemiology
• Safety Audits and Inspections

Additional safety-related events

• Drug Safety and Pharmacovigilance Across the Product Lifecycle | October 22-24 | April 8-10
• Benefit-Risk Assessment and Management Across the Lifecycle | November 5-6
• Safety Risk Communication for Medical Products | November 7-8
• Pharmacovigilance and Risk Management Strategies Conference | January 28-30

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