Description
The MDR 2017/745 defines in its Annex 14, B the requirements for a Post-Market Clinical Follow-Up (PMCF) for higher class medical devices. Find here the template to cover the aspects of a PMCF plan.
PMCF Plan template for MDR 2017/745
CHF49.00
The Medical Device Regulation MDR 2017/745, Annex 14, B defines requirements for manufacturers to conduct post-market clinical follow-up studies for higher classed medical devices. Find here the template for the PMCF plan. The plan is delivered as:
- Word file format
- Requirements per MDR 2017/745
