Central Drugs Standard Control Organization Directorate General of Health Services, Ministry of Health and Family Welfare, Government of India THIS  SITE PROVIDE GENERAL INFORMATION ABOUT DRUG REGULATORY REQUIREMENT IN INDIA  Home Site Map Archive Feedback Downloads Contact  Search : About Us Central Drugs Standard Control Organization  NEW!!  State Drugs Control Organization Organizational Chart   Import of Drugs Clarification in r/o Import of Notified Medical Devices  Re-Registration Circulation letter  Import of Drugs for Personal use  Drugs for marketing in India Imported Formulations  Registered NEW!! Bulk Drugs Registered NEW!! Vaccines Registered  NEW!! Medical Devices & Blood ProductsNEW!! Registration Application Received    NEW!! Renewed Registration Bulk Drugs &  Formulation  NEW!! Clinical Trials Global Clinical Trials   Global Clinical Trials NEW!!  Manufacturing Units Having WHO GMP Certification New Drugs Approved for Marketing in India NEW!! Permission to Market in India Diclofenac for veterinary use Drugs Banned in India ADDITIONAL CLARIFICATION FOR IMPORT REGISTRATION OF MEDICAL DEVICESNEW!! GUIDELINES FOR IMPORT AND MANUFACTURE OF MEDICAL DEVICES FURTHER UPDATE ON GUIDELINES OF MEDICAL DEVICES CLARIFICATIONS ON GUIDELINES FOR IMPORT & MANUFACTURE OF MEDICAL DEVICES FURTHER CLARIFICATIONS ON GUIDELINES FOR IMPORT & MANUFACTURE OF MEDICAL DEVICES ON 30/8/06 NEW!!!! IMPORT REGISTRATION CERTIFICATES ISSUED UPTO Sept. 2008 NEW!! List of licensed Indigenous Manufacturers of Medical Devices upto 30-Oct, 2008 NEW!! Current Topics  Training & Workshops Information    GCP Workshops Related Links Vacancies OFFICE ORDER Public Notice -- medical device regulation   Daily Despatch Details   EXPORT OF CLINICAL TRIAL SAMPLESNEW!!                       Rules & Regulation Laws For Drugs & Cosmetics Drugs & Cosmetic Act & Rules Notification  NEW!!  Central License Approving Authority Blood Bank & its Products NEW!! LVP, Vaccine & Sera Guidance to applicants for LVP Manufacture Other Topics Goods Manufacturing Practices Mashelkar Committee Report   Consultation for Review of Guidelines  Narcotic & Psychotropic Substance National List of Essential Medicines Good Clinical Practice Pharmacovigilancae List of Diagnostic Kits for Blood Bank   Biologicals Guidance For IndustryNEW!! Submission of Clinical Trial Application for Evaluating Safety and Efficacy Requirements for permission of New Drugs Approval Post approval changes in biological products:Quality safety and Efficacy Documents Preparation of the Quality Information for Drug Submission for New Drug Approval:Biotechnological/Biological Products Drugs Banned in India   DISCLAIMER