Blogs
China’s CMDE Announces New Regulation…
The Center of Medical Device Evolution (CMDE) of China has released a regulation (notification 53) th…
An Overview of European Unique Device…
The Medical Device Regulations (EU 2017/745, EU 2017/746) introduce the Unique Device Identification …
Medical Device Post Market Surveillance
The post-market surveillance (PMS) systems that monitor medical device safety after launch reduce bot…
Why is Medical Technology Getting Shr…
Cybersecurity threats top the list when it comes to imminent dangers surrounding the healthcare indus…
Labeling Requirements for Medical Dev…
Labeling acquires a major part when it comes to ensuring the safety of those that are using it. The l…
IMDRF Offers Final Clinical Guidelines
The International Medical Device Regulators Forum (IMDRF) released three final documents covering cli…
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