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- W2884455157 abstract "Marketing authorization of medical devices in India is given under heading “Registration Certificate and it is as per the regulatory processes in other countries. The foreign companies marketing of medical devices require either own office or an agent to receive, store and distribute the devices. The marketing Authorization (Registration Certificate) is considered valid for three years from the date of its issue. Only the Notified Medical Devices, New medical Devices and the devices classified under drug rules require marketing Authorization from DCGI. The other medical devices e.g. Non-notified devices do not require manufacturing, sales, import registration and can be marketed freely." @default.
- W2884455157 created "2018-08-03" @default.
- W2884455157 creator A5018005593 @default.
- W2884455157 date "2018-02-13" @default.
- W2884455157 modified "2023-09-23" @default.
- W2884455157 title "REVIEW OF MARKETING AUTHORIZATION OF MEDICAL DEVICES IN INDIA" @default.
- W2884455157 doi "https://doi.org/10.22270/ijdra.v2i4.150" @default.
- W2884455157 hasPublicationYear "2018" @default.
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