Top Industry News
- Swiss Public Consultation for ICH Guideline E6(R3) "Good Clinical Practice (GCP)" Opened in Switzerland
- Australia New Zealand Food Standards Code – Standard 2.9.1 – Infant Formula Products
- FDA Drug-Drug Interaction Assessment for Therapeutic Proteins Guidance for Industry
- ANVISA - Do You Want to Know If a Clinical Research is Authorized by ANVISA?
- MHRA - Register Medical Devices to Place on the Market
- Indonesia’s BPOM Conducts Wave of Internal Audits of Quality Management Systems
- UK Shares Biological Security Strategy, Makes Shaping Regulations an Indicator of Success
- Swissmedic - Adaptation of the Guidelines for Authorization of Homeopathic Medicinal Products, Anthroposophic Medicinal Products and Other Complementary Medicinal Products
- MHRA Implementation of Medical Devices Future Regime
- FDA - Content of Premarket Submissions for Device Software Functions
- MHRA Medicines: Apply for a Parallel Import Licence
- MHRA Regulating Medical Devices in the UK