The Central Drugs Standard Control Organization (CDSCO) is the national regulatory body for Indian pharmaceuticals and medical devices. Under the direction of the Ministry of Health & Family Welfare, the CDSCO is responsible for the approval of drugs, conducting clinical trials, laying down the standards for drugs, control over the quality of imported drugs in the country, and coordination of the activities of State Drug Control Organizations by providing expert advice. The website serves as a comprehensive resource for regulatory guidelines, drug approvals, and public notices related to pharmaceuticals and medical devices in India.
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Domain Rating
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Domain Authority
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Citation Level
1940
English, etc
Website Key Features
Drug Approval
Provides information on the process and status of drug approvals in India.
Clinical Trials
Offers guidelines and updates on clinical trials conducted within the country.
Regulatory Guidelines
Detailed regulatory guidelines for pharmaceuticals and medical devices.
Public Notices
Latest public notices and announcements from the CDSCO.
Import/Export
Information on the regulation of imported drugs and medical devices.
State Drug Control
Coordination and support for State Drug Control Organizations.
Online Services
Access to online services for drug approval and clinical trial applications.
Publications
Access to publications, reports, and annual reports by CDSCO.
Contact Information
Direct contact details for various departments within CDSCO.
Similar Sites and Competitors
Additional information
Headquarters
New Delhi, India
Parent Organization
Ministry of Health & Family Welfare, Government of India
Key People
Drugs Controller General of India (DCGI)
Mission
To safeguard and enhance public health by assuring the safety, efficacy, and quality of drugs, cosmetics, and medical devices.
Vision
To be a leader in the regulation of pharmaceuticals and medical devices, ensuring access to safe, effective, and quality products for the public.
Online Portal
The website also features an online portal for submissions and tracking of applications related to drug approvals and clinical trials.
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