Detailed Analysis 2021 - Post-Market Activities in the EU-MDR — A Detailed Analysis Virtual Training

Post Market Activities are a GMP regulatory requirement for the medical device industry in both the US and European Union. These activities provide a valuable system for obtaining data and continuous feedback about a medical device that is on the market.
What are the key elements of a PMS system?
How should a PMS system function?
What is the role of risk management in PMS?
Key compliance dates
Transition from Re-active to Pro-active
Data Inputs and Collection Methods
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Speaker:
Ms. Thomas has over two decades of cGMP hands-on industry experience in both pharmaceutical and medical device manufacturing operations.