Requirements of the medical device regulation (MDR) for CE marking training course >
Learn about the key requirements, concepts, and the overall process for CE marking under the Medical Devices Regulation (MDR).
CE marking is the medical device manufacturer’s claim that a product meets the General Safety and Performance Requirements (GSPR) of all relevant European Medical Device Regulations and is a legal requirement to place a device on the market in the European Union.
Given the stringent requirements on patient safety and device performance, accessing the European market brings challenges that can delay your product launch.
Discover our CE marking dedicated training portfolio, developed to increase your understanding in navigating the CE Certification process and to increase your readiness for market.