NSF Winter Camp 2027 - Medical Device Regulatory Affairs in a Compact and Practical Format
This training programme will be delivered in German language only.
From 22 to 26 February 2027, the NSF Winter Camp provides a structured introduction to the fundamentals of Medical Device Regulatory Affairs. During five days of in-person training, participants will gain an overview of the MDR and learn how to apply key regulatory requirements throughout the medical device lifecycle.
The programme combines expert input with practical workshops, case studies and opportunities to exchange experiences with Regulatory Affairs and Quality professionals from the MedTech community. Topics include device classification, technical documentation, clinical evaluation, quality and risk management, usability, software, cybersecurity, PMS and vigilance.
Download the full Winter Camp agenda: Agenda (German) .
Who Should Attend
510(k) Premarket Notification Workshop – Bringing Medical Devices to the U.S. Market
AI Act, MDR/IVDR, QMSR: Practical AI compliance trainings for medical devices
AI in Medical Devices - Expectations in a Maturing Field
Biological Evaluation of Medical Devices - How to Succeed in Your Notified Body Assessment
CAPA Considerations: A Comprehensive Overview
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