Malaysia Consults On Medical Device Risk Classifications
A 20-day consultation on the risk classification of medical devices intended for the Malaysia market ends on 28 February
You may also be interested in...
Stay current on regulatory guidelines from around the world with Medtech Insight's Guidance Tracker. Thirty-six documents have been posted on the tracker since its last update.
The Malaysian government has finalised its much-awaited medical device regulations, paving the way for the implementation of new mandatory requirements from 1 July 2013.
In its just-released real-world evidence framework, NICE assesses the role and value of data collected outside highly-controlled clinical studies in driving more innovation towards health care professionals.