Top Industry News
- PMDA Method for Submission of Documents for Conformity Assessment of Generic Drugs for Prescription Through the Gateway System" Was Posted
- FDA M11 Clinical Electronic Structured Harmonised Protocol
- Malaysia Revises Device Law to Require Filings for License Renewal 90 Days Before Expiry
- FDA Controlled Correspondence Related to Generic Drug Development
- Anvisa Simplifies the Regulatory Flow for the Publication of Periodically Updated Rules
- TGA Access Generic Medicines Work-Sharing Initiative Update
- EMA Facilitating Decentralised Clinical Trials in the EU
- SFDA Guidance for the Operation and Use of Radiation Emitting Medical Devices (MDS – G007)