Post-market surveillance is critical for ensuring continued safety and effectiveness of a medical device throughout its lifecycle.
It is also a regulatory requirement.
Yet it proves to be challenging in practice to implement a systematic process for collecting and analyzing data for identifying safety signals and taking timely action.
In this free video lesson from our fully on-demand ISO 14971 certification course, I explain the requirements for collecting and analyzing post-market data according to Clauses 10.3 and 10.3.
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Take 30% off regular price when you register by January 8, 2025.
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