Description: Post Market Clinical Follow Up (PMCF) Surveys are a hot topic among those working on Medical Device Regulation (MDR) submissions. With there being a lack of documented guidance around PMCF surveys, this webinar will enable the audience to better understand when to consider PMCF surveys as an appropriate data collection method, which survey approach (Level 8 vs. Level 4) to take and how to effectively design a PMCF survey protocol that will allow for effective survey implementation.
Learning Objectives:
Understand the importance / role of PMCF within the EU-MDR• Learn about the differing PMCF Survey approaches (Level 4 vs. Level 8)
Learn about the differing PMCF Survey approaches (Level 4 vs. Level 8)
Take away key learnings / considerations for how to plan a PMCF Surve
