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Top Industry News
- SFDA - Guideline on Good Pharmacovigilance Practices (GVP)
- ANVISA Launches Internal Virtual Assistant
- NMPA Announcement on Putting into Use the Electronic Certificates of Documentation for Export of APIs to EU and Certificate of a Pharmaceutical Product
- MHRA Marketing Authorisation Holders' Submission of Nitrosamine Risk Evaluation, Risk Assessment and Confirmatory Testing
- PMDA - Consultation Services for Pharmaceuticals and Quasi-Drugs
- India’s NPPA Shares Fixes for Problems with Implementation of Pharmaceutical Database
- Pakistan’s DRAP Signs Agreement to Use Integrated Electronic Platform for Regulatory Forms
- PMDA - Information on Online Submission Using the Electronic Application Data System Has Been Posted
- MHRA - Application of the Falsified Medicines Directive: Safety Features in Northern Ireland
- MHRA European Commission (EC) Decision Reliance Procedure
- FDA Referencing the Definition of "Device" in the Federal Food, Drug, and Cosmetic Act in Guidance, Regulatory Documents, Communications, and Other Public Documents