Back to R2 link
Top Industry News
- SWISS Adaptation of the Forms for the New Authorization and the Change of Human and Veterinary Medicinal Products
- Europe Reform of the EU Pharmaceutical Legislation
- MHRA Regulating Medical Devices in the UK
- FDA Center for Veterinary Medicine (CVM) GFI #108 Registering with CVM’s Electronic Submission System
- ANVISA Updates the Brazilian Pharmacopoeia Phytotherapy Form
- SWISS Adaptation of the guideline GMP Conformity of Foreign Manufacturers and Form Declaration of the Technically Responsible Person for Foreign manufacturers
- FDA S12 Nonclinical Biodistribution Considerations For Gene Therapy Products
- MHRA Register Medical Devices to Place on the Market
- Team-NB Updates Best Practices for MDR Technical Documentation Submission
- Pakistan Freezes Fees for Major Pharmaceutical, Medical Device Regulatory Services