- Draft Guidance of New Registration Requirements For Medical Devices.
- Guidance on Requirements for Unique Device Identification (UDI) for Medical Devices
- MRG is proud be to assigned by Hologic BVBA to be their Authorized Representative on behalf of the manufacture in dealing with the SFDA
- Updates on medical device marketing authorization (MDMA) procedure following United Kingdom leaving European Union (Brexit)
- Newsletter – Issue 12