Top Industry News
- SFDA- Templates for SPC, PIL and Labelling
- FDA- Providing Regulatory Submissions in Electronic Format – Certain Human Pharmaceutical Product Applications and Related Submissions Using the eCTD Specifications
- EU Begins Transition to Electronic Product Information for Medicines
- MHRA- UK and Russia sign MoU on Regulatory Cooperation on Medicines
- EMA Updates Brexit Guidance
- FDA- Safety and Performance Based Pathway
- FDA- Marketing Status Notifications Under Section 506I of the Federal Food, Drug, and Cosmetic Act; Content and Format
- MHRA Guidance and Publications on a Possible no Deal Scenario
- GS1 Guidance to Support Point-of-Care Scanning of UDI Data for Implantable Devices
- TGA- Guidelines on the Evidence Required to Support Indications for Listed Complementary Medicines