| REGULATORY UPDATE: India Central Drugs Standard Control Organisation releases "Guidance Document on Common Submission Format for Registration of Medical Devices in India"
The India Central Drugs Standard Control Organisation has posted new documents for download including:
"Guidance Document on Common Submission Format for Registration of Medical Devices in India"
"Requirements for conducting clinical trials of devices in India."
If you are selling devices in India, you may want to bookmark this page: http://cdsco.nic.in/
I posted this announcement on the Health Sciences LinkedIn group last week. Join your colleagues who are already part of the global Health Sciences-Underwriters Laboratories LinkedIn group
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