Overview: The Korean Ministry of Food and Drug Safety (MFDS), formerly known as the Korea Food & Drug Administration (KFDA), is the main regulatory body

Consultation Meeting With Korean Health Authority (MFDS) In South Korea, the Ministry of Food and Drug Safety (MFDS) offers pharmaceutical, biotech and food companies, different

Clinical Trial Applicaiton (CTA) in china In China, a Clinical Trial Application (CTA) should be submitted to the National Medical Products Administration (NMPA), to request

Registration of Drug Master File (DMF) in South Korea The Ministry of Health and Food Safety (MFDS) requires manufacturers and importers of certain Active Pharmaceutical

PMDA Consultation meeting in Japan Pharmaceuticals and Medical Devices Agency (PMDA), the Japanese Regulatory Authorities, offers pharmaceutical and biotech companies, different types of consultation meetings,

Registration of Drug Master File (DMF) in Japan In Japan, Drug Mater File (DMF), known as Master File (MF), is a system that was introduced