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CDSCORegistration

Under the drugs and cosmetics act. CDSCO is responsible for approval of new drugs, conduct of clinical trials , laying down the standards for drugs control over the quality of imported drugs in the country and coordination of the activities.

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Step 1

Documentation.

Step 2

Applicaton Filling.

s

Step 3

Grant of CDSCO Registration.

Overview

Divisions

Processs

Documents Required

FAQ

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CDSCO Registration overview

CDSCO is the National Regulatory Authority for Indian pharmaceuticals and medical devices under the Directorate General of Health Services, Ministry of Health and Family Welfare in India.It is the responsibility of CDSCO for approving new drugs and conduct of clinical trials in India under the Drugs and Cosmetics Act, 1940 (“Act”) and Drugs and Cosmetics Rules, 1945.

What Are The Divisions Of CDSCO Registration?

(1) Cosmetics

(2) DCC-DTAB

(3) BA/BE

(4) Medical Devices and Diagnostics

What is the Process of CDSCO Registration

(1) Gather the required documents

(2) File and submit the cdsco online application

(3) Wait for the cdsco's assessment of the application

(3) Getting the registration number for cosmetics import

Documents Required For CDSCO Registration?

(1) Power attorney.

(2) Undertaking and declarations.

(3) Ingradient Details.

(4) Product label.

(5) License and certification

(6) Licensing fee

(7) Testing Report

FAQs

(1) What is CDSCO Registration?

(2) Who approved medical device in india?

(3) How much time is required for the development of new drug?

(4) Is CDSCO Statutory?

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