Top Industry News
- FDA Adds Submission Type to Delayed eCTD Implementation Requirements
- EMA- Updated rules for clinical development of vaccines
- FDA- Clinical Trial Imaging Endpoint Process Standards Guidance for Industry
- TGA- GMP clearance process improvements - Post implementation update
- MHRA- Good laboratory practice (GLP) for safety tests on chemicals (Updated)
- FDA- Multiple Function Device Products: Policy and Considerations
- Biosimilars: Experts Discuss Possible Interchangeability Guidance Changes and Reducing Phase 3 Requirements