Vigilance, post-market
Advance your expertise in vigilance, post-market surveillance (PMS) and complaint management for medical devices. Gain practical knowledge of regulatory reporting, signal detection and post-market clinical follow-up (PMCF).
Strategic Regulatory Affairs under the MDR
Regulatory strategy under the MDR calls for well-structured authority interactions, efficient internal processes, and the ability to identify and assess regulatory developments at an early stage. This…Language: English
FDA MedTech Regulatory Update 2026
Get a compact update on key FDA requirements for medical devices in 2026 and practical guidance for your U.S. planning in 2027. The seminar covers regulatory pathways, FDA interaction, QMSR, clinical…Language: English
Contact
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Our professional development portfolio is extensive. We would be pleased to discuss your requirements with you personally and help identify the most suitable options from our range of offerings. Let our professional development experts advise you and feel free to contact us today.
Verena Planitz
Conference Manager Healthcare
+49 6221 500-655
v.planitz@forum-institut.de