Why AE Consulting
- Extensive expertise in medical device studies and implant trials
- Professional experience with start-up companies
- Competent experience in various project support for medium and large companies
- Extensive knowledge of Post-Market Clinical Follow-up, PMCF.
Post-Market Clinical Follow-Up (PMCF) is the ongoing process of actively collecting of clinical data on the safety and effectiveness of medical devices after CE approval.
PMCF is one of the regulatory requirements, which is specified in the Medical Device Regulation (MDR).