Top Industry News
- Malaysian Guidance Document on Voluntary Good Pharmacovigilance Practices (Gvp) Inspection
- Denmark puts better use of data and new technology at heart of new regulatory plan
- SFDA Requirements of Shipments Clearance at Ports of Entry
- EMEA MDCG adds guidance on legacy devices, Eudamed to IVDR to-do list
- ICH Drafts Guideline on Pediatric Extrapolation in Drug Development
- TGA updates medicinal cannabis quality rules
- FDA Cybersecurity in Medical Devices: Quality System Considerations and Content of Premarket Submissions
- MHRA Early access to medicines scheme applications: pending, refused, granted
- FDA E8(R1) General Considerations for Clinical Studies