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Indian regulators propose changes to good manufacturing practice requirements for medical devices

December 8, 2014 by MassDevice

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.

Emergo Group

By Stewart Eisenhart, Emergo Group

India's Central Drugs Standard Control Organization (CDSCO) has proposed bringing the country's Good Manufacturing Practice requirements for medical and in vitro diagnostic devices more in line with those of the ISO 13485 quality management system standard.

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