MDCG publishes MDR Surveillance Guidelines
MDCG publishes MDR surveillance guidelines regarding the transitional provisions under Article 120 of the MDR with regard to devices covered by certificates according to the MDD or the AIMDD.
MedTech
Irish NSAI Expects Approval to get EU MedTech Certification
The Irish NSAI expects approval to get the EU MedTech
Compliance And The Growth Of The Medical Industry
Compliance and the growth of the medical industry, does it work together? This question is highly relevant because the growth in the medical device industry is significant. And also, this will continue to be the case for the foreseeable future.