Top Industry News
- FDA-Reporting Amount of Listed Drugs and Biological Products Under Section 510(j)(3) of the Federal Food, Drug, and Cosmetic Act; Draft Guidance for Industry
- MHRA-Register medical devices to place on the market
- Malaysia-Updates guideline for registration of drug-device combination products
- MHRA-Clinical trials for medicines: apply for authorisation in the UK
- EMA-Regulatory update - EMA encourages companies to submit type I variations for 2021 in November 2021
- SFDA-Products Classification Guidance
- EMA-Publishes guideline on running registry-based studies
- MHRA-Export medical devices
- MHRA-Clinical trials for medicines: Manage your authorisation, report safety issues