If you need to gain in-depth knowledge on the best way to collect and report adverse events and safety data and manage the risk associated with and risk to your products, then this is the course for you. Its unique format will provide you with the key skills and knowledge needed to operate a fast, effective drug safety programme.
Work to international standards and meet regulatory requirements for product safety
Understand the link between your product safety documentation;
Effectively monitor your products’ benefit risk profiles and follow up on key signals;
Prepare accurate Periodic Benefit Risk Evaluation Reports (PBRER) to keep track of ADRs.
From: July 10, 2014 09:00
To: July 11, 2014 17:00
Radisson Blu Edwardian Grafton Hotel, 130 Tottenham Court Rd, W1T 5AY, United Kingdom