Top Industry News
- Malaysia Withdrawal Of Medical Device Registration (New And Re-Register) And Change Of Notification Application
- ANVISA Easter Must Bring Products that Comply With the New Labeling Rules
- FDA Framework for the Use of Digital Health Technologies in Drug and Biological Product Development
- SFDA Guidance on Manufacturing Paths of Medical Devices and Supplies (MDS-G011)
- SWISS Technical Adaptation of the CPP Order Form and New Version of the CPP Request Guide
- Pakistan Gives Manufacturers 30 Days to Update Finished Product Specifications in Online Portal
- SDFA Guidance on MDMA –Significant and Non-Significant Changes (MDS-G012)