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Listen "S5 E8: Academy Talks: Medical Device Documentation: Post Market Surveillance"
Episode Synopsis
As a startup company, post market surveillance can feel far away and not relevant, but key documents are of critical importance to develop during the device development process. The authorities expect companies to have a PMS procedure available and plans for surveillance of PMS and PMCF. We will walk through which active and passive collection methods are available for use to ensure the manufacturer has the data available to fulfil the requirements.
More episodes of the podcast The Qmed Podcast
Academy Talks: Medical Device Documentation
23/10/2024
S4_E2_PMCF survey with CETAS Healthcare
08/02/2024
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