Top Industry News
- ANVISA- Document Organization Guide Common Technician (CTD) For Registration and Post-Registry Medicinal Products
- Health Canada- Biopharmaceutics Classification System Based Biowaiver
- ANVISA- New GMP Regulatory Framework Approved
- TGA- Proposal to Introduce a Unique Device Identification (UDI) System for Medical Devices in Australia
- SFDA- Guidance on Requirements for Reporting of Incident and Adverse Event of Medical Devices