All Videos
Non-EU Manufacturers: Appointing an Authorized Representative (EC-REP) for Medical Devices and IVD`s
Discover how MedNet EC-REP GmbH simplifies EU compliance for medical device and IVD manufacturers with authorized representative and seamless registration services.
Regulatory Importer Service for Medical Devices Explained
Discover how MedNet EC-REP’s Regulatory Importer Service streamlines EU market access for medical devices. This video explains the role and responsibilities of an importer. Learn how our service ensures seamless, compliant shipments to your European customers.
Responsible Person under the EU Cosmetic Products Regulation 1223/2009
Responsible Person under the EU Cosmetic Products Regulation 1223/2009
The new General Product Safety Regulation GPSR - How does it complement MDR?
In this insightful presentation from Medica 2024, Dr. Stephanie Vorwerk of MedNet EC-REP GmbH dives into the essential updates surrounding the new General Product Safety Regulation (GPSR) and its relationship with the Medical Device Regulation (MDR).
.avif&w=1920&q=75)
.avif&w=1920&q=75)

