Top Industry News
- EMA starts requiring registration of new sites for centrally authorized medicinal products
- ANVISA approves new regulatory framework for low-risk drugs subject to notification
- TGA Consultation on potential regulatory options for 'export only' biologicals
- SFDA A Guide for Licensing Consulting Services Establishments
- MHLW Pharmaceuticals and Medical Devices Safety Information
- TGA - registration of new generic medicines and biosimilar medicines
- TGA Medical device incident reporting (MDIR) guide
- SFDA Food Clearance Conditions and Requirements
- TGA -registration of new chemical entities in Australia
- TGA -new or extended uses, or new combinations of registered medicines
- SFDA Guidance for Borderline Products Classification