Top Industry News
- FDA Extends compliance date for submitting DMFs in eCTD format
- EMA-Optimising safety information for medicines in Europe throughout product lifecycle
- TGA-Changes to submission of ADR reports for unapproved medicines and biologicals
- TGA-Data Management and Data Integrity (DMDI)
- SFDA-Guidance on Importation Requirements for Distillation Apparatuses
- CFDA adjusts some administrative approval procedures for drugs and medical devices
- MHRA-Good laboratory practice (GLP) for safety tests on chemicals (Updated)
- TGA-Varying biological entries on the ARTG