India Mandates Online Registration for Medical Devices

India’s Central Drugs Standard Control Organization, responsible for overseeing the country’s medical device market, has implemented an online portal for submission of registration certificates and import licenses to facilitate faster commercialization pathways.

This online registration applies only to notified medical devices, and from April 1 this registration will be mandatory.

This portal will be useful for:

  • Patients who can learn about drug or device approvals
  • Industry that can upload essential documents
  • Consumer who can search registered drugs and get more user-related information on them

Authorized Agents can submit Form-41 registration certificates and Form-10 import licenses, as well as track the progress of registration applications on the Central Drugs Standard Control Organization Website.

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Posted on by Gunjan Bagla
Gunjan Bagla
California-based management consultant Gunjan Bagla runs Amritt, a consulting firm helping American companies to succeed in India. Amritt is the trusted advisor for India market research, India business development, India market entry, Global Engineering, Global Technology Scouting, India R&D and Open Innovation. Gunjan is author of "Business in 21st Century India: How to Profit Today from Tomorrow’s Most Exciting Market" (Hachette Book Group, 2008), Amazon's top rated title on the subject. He has appeared as the India Expert on BBC Television, Bloomberg TV, Fox Cable Business and has been quoted in the New York Times, the Los Angeles Times, the Hollywood Reporter and Business Week for his expertise on India.

1 comment

1 Jonam { 05.19.16 at 9:37 PM }

Good things are on its way, its a significant act to come up with a portal like this to make it easier to know and get an idea about the submission,registration and other information. I am also sharing this below, which explains in brief about the Online Portal for CDSCO

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