Top Industry News
- SWISS Adjustments to the Guidelines for Medicinal Product Information for Medicinal Products for Human Use
- Europe Notified Bodies Create Best Practice Guide for Submitting IVDR Technical Documents
- Malaysia’s MDA Creates Online Payment System for Medical Device Regulatory Services
- SWISS New Guidelines on Mobile Technologies for Human and Veterinary Medicinal Products
- MHRA Human Medicines: Register of Electronic Export Certificates
- Pakistan DRAP Seeks Feedback on Planned Changes to Drug Research Regulations
- FDA Q13 Continuous Manufacturing of Drug Substances and Drug Products