Drug Controller General of India
This article needs more links to other articles to help integrate it into the encyclopedia. (February 2014) (Learn how and when to remove this template message)
Drug Controller General of India under the gamut of Central Drugs Standard Control Organization is responsible for approval of licences of specified categories of drugs such as blood and blood products, IV fluids, vaccines and sera in India. Drug Controller General of India, comes under the Ministry of Health & Family Welfare. 
The current DCGI is Dr. S. Eswara Reddy 
Former DCGIs include Dr. G.N. Singh.
DCGI lays down the standard and quality of manufacturing, selling, import and distribution of drugs in India.
- Acting as appellate authority in case of any dispute regarding the quality of drugs.
- Preparation and maintenance of national reference standard.
- To bring about the uniformity in the enforcement of the Drugs and Cosmetics Act.
- Training of Drug Analysts deputed by State Drug Control Laboratories and other Institutions
- Analysis of Cosmetics received as survey samples from CDSCO (central drug standard control organisation)
With the notification of Medical Device Rules 2017 by the Government of India, DCGI will also act as Central Licensing Authority (CLA) for the medical devices which fall under the purview of these rules. Out of four Classes of medical devices from Class A to Class D, DCGI will be the direct licensing authority for Class C and D devices, whereas it will coordinate licensing for Class A and B devices through State drug controllers, who will act as State Licensing Authority or SLA. <Medical devices Rules, 2017_gsr78E>
Zonal Offices Of CDSCO(Central Drugs Standard Control Organisation)
The central government have established 4 zonal offices of CDSCO at Mumbai, Kolkata, Chennai, and Ghaziabad, various Sub-Zonal offices and Port offices, which works in close collaboration with the state control administration and assist them in securing uniform enforcement of the Drug Act.
- CENTRAL DRUGS STANDARD CONTROL ORGANIZATION (accessed on 18 Oct 2014)
- 4 SEP, 2012, ET BUREAU, Economic Times Pharmaceutical companies told to submit safety reports on new drugs every 6 months (accessed on 4 Sept 2012)
|This article about an organisation in India is a stub. You can help Wikipedia by expanding it.|