Top Industry News
- SFDA- Guidance on Requirements for Electronic Instructions for Use (e-IFU) of Medical Devices
- EDQM Updates Two Guidelines on the CEP Procedure
- SAHPRA- Roadmap and Transitional Process for the Regulation of Complementary Medicines
- ANVISA- Published AIR Report on Nutrition Labeling
- SAHPRA- Naming and Labelling Conventions for Active Ingredients in Complementary Medicines
- FDA- Providing Regulatory Submissions for Medical Devices in Electronic Format - Submissions Under Section 745A(b) of the Federal Food, Drug, and Cosmetic Act
- MHRA Explains Exceptions and Modifications to EU GVP in No-Deal Brexit
- FDA- Changes to Existing Medical Software Policies Resulting from Section 3060 of the 21st Century Cures Act
- FDA- Policy for Device Software Functions and Mobile Medical Applications
- SFDA- Medical Devices Interim Regulation
- FDA- Medical Device Data Systems, Medical Image Storage Devices, and Medical Image Communications Devices
- FDA- New MAPP Offers Insight Into Patient-Oriented Labeling Consultations for Combination Products