Central Drugs Standard Control Organization
Directorate General of Health Services, Ministry of Health and Family Welfare, Government of India

Home About us Archive Feedback Downloads RTI Contact           Photogallery 
Gazette Notification G.S.R 16(E) Dated 13.01.2014        Notice-Meeting of the Pharmaceuticals Industry Associations        Report of 46th DCC Meeting        Draft Guidelines on AV Recording of Informed Consent Process in Clinical Trial        Approval of Bio Analytical Laboratory for BA/BE Studies        DCG(I)'s New Year Message        Medical device alert (ASR XL)        Audio-Video Recording of Informed Consent Process of All New Subjects in Clinical Trials- Administrative Orders        Induction Training Courses for Drugs Inspectors        Induction Training Courses for Drugs Inspectors        GSR No.588(E) dt.30.08.13 regarding Schedule H1        GSR 590(E)        GSR No.589(E)        Formula to Determine the Quantum of Compensation in the Case of Clinical Trial related SAEs of Deaths Occuring during Clinical Trials        Furnishing of information in respect of financial support, fees honorarium, Payments in kind etc to be paid to the investigators as per contract        
Actions on the Recommendations of Prof. Ranjit Roy Chaudhury Expert Committee        Report of Prof. Ranjit Roy Chaudhury Expert Committee        Report of Prof.C.K.Kokate on Fixed Dose Combinations        Procedures for permissions to import small quantities of Drugs For Personal Use        
Rules & Regulation
Ethics Committee Registration
Vaccine Permission, Recall & Suspensions
New Drugs
Clinical Trial
Medical Devices
Blood Bank
Test Licences
Traditional Drugs
AEFI / Pharmacovigilance Programme of India (PVPI)
Haemovigilance Programme
Recommendations of DTAB, DCC and IND Committee
Recommendations Of NDAC and MDAC
Written Confirmation for Export of API to EU
Updated List of Fixed Dose Combinations approved by DCG(I)
Updated List of New Drug approved for marketing in India
Court Orders


Drug Alert - Drugs declared as NSQ by Central Laboratories.
Procedures for Permission to Import Small Quantities of Drugs For Personal Use
National Formulary of India 2011

Information: Ensuring rights/Safety of Clinical Trials Subjects in India

Drugs banned in the Country
 Central License Approving Authority
 Data Bank 
Mashelkar Committee Report  
Spurious Drugs
Miscellaneous/Tender Notices

Related Links

Notices / Office Order
Gazette Notifications
Apex Committee recommendation: CT Status
Minutes of the Expert Committee Meeting   
Prioritization of Activities at CDSCO
Checklist for Pre-Screening of Application
Scanned  Copy Initiatives & Achievements of CDSCO

Daily Dispatch Details 2014

Four years Achievements of CDSCO (2009 -2013)
Daily Dispatch Details 2013

Site visited hit counter Times