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.
