Post-Market Clinical Follow-Up

As part of the clinical evaluation, the MDR requires manufacturers to plan and carry out suitable PMCF activities. Here the spectrum ranges from well-structured customer surveys to PMCF studies. Good data quality, compliance with data protection requirements and ethical issues are essential.

Based on our extensive experience, we offer you tailor-made solutions for your medical device. A corresponding PMCF strategy can also be developed if we prepare the clinical evaluation of your product for you and include your current PMS / PMCF data there.

To get started with the topic of PMCF or to deepen your knowledge, we offer a seminar that provides you with comprehensive information on the topic of PMS / PMCF.