divendres, 18 de juliol del 2014

Indian regulators clarify requirements for medical device registrations, clinical trials




The Emergo Group Blog provides short updates on quality and regulatory topics that may be of interest to QA/RA professionals in the medical device and IVD industry. No fluff, just straight to the point. We hope you'll enjoy the content.





Indian regulators clarify requirements for medical device registrations, clinical trials

By Stewart Eisenhart, Emergo Group


New orders from the Indian Ministry of Health & Family Welfare's Central Drugs Standard Control Organization (CDSCO) clarify some requirements regarding the country's sometimes opaque medical device registration and clinical trial regulations.




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