Peercode and Medace's first live MDR and quality management system training for professionals took place on May 18, 2022 in Maastricht
Peercode and Medace have organised a one day training session explaining Regulatory legislation, applicable International standards and requirements of the Technical File of Medical Devices that are certified under the Medical Device Regulations (MDR).
The full-day training workshop has according to participants been a great introduction to Medical Device Regulation and Quality Management System requirements according and to International standard EN ISO 13485:2016. Participants have gained in-depth knowledge on key topics regarding Medical Device Regulation and Certification processes such as Risk Assessment, Post Market Surveillance, development of Clinical Report, Testing and Verification which will strongly support their current and future product development. This interactive training tool place at the Medace facilities in Maastricht.
