Top Industry News
- MHRA Guidance on qualified person responsible for pharmacovigilance (QPPV) including pharmacovigilance system master files (PSMF)
- SFDA Regulation and Requirements for Conducting Clinical Trials on Drug
- MHRA Notify the MHRA about a clinical investigation for a medical device
- FDA expands eSTAR filing to de novo devices, IVDs
- TGA Prescription medicines: applications under evaluation
- FDA offers draft guidance for registries as RWD
- TGA Australian manufacturing licences and overseas GMP certification