Top Industry News
- Health Canada Submission Filing Requirements - Good Manufacturing Practices (GMP)/Drug Establishment Licences (DEL)
- SFDA-Guidance on Importation Requirements for Medical Devices and Non-Medical IVDs Intended for Educational or Non-Clinical Research Purposes
- PMDA - Pharmaceuticals and Medical Devices Safety Information
- EMA post-authorisation procedural advice for users of the centralised procedure
- India adopts New Medical Device Regulations
- FDA - Improving Communication of Important Safety Information(Guidance for Industry)
- PMDA Head Talks Priorities for 'Rational Medicine'
- FDA Details Combination Product Postmarket Safety Reporting Requirements
- MHRA Looks to Increase Medical Device Fees