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  1. The Directorate General of Drug Administration (DGDA) under the Ministry of Health & Family Welfare, Government of the People's Republic of Bangladesh, is the Drug Regulatory Authority of the country. This DGDA supervises and implements all prevailing Drug Regulations in the country and regulates all activities related to import, procurement of ...

  2. statedrugs.gov.in › SFDA › HomepageONDLS|CDSCO

    Third Party Licence Verification. Mechanism to verify any licnece issued by ONDLS Pan india.....Verify Now

  3. New Applications. Submit Your New Applications HERE! Check the Status of My Applications. EMAIL ADDRESSES ARE REQUIRED. Registrants must have a current and active email address listed on their registration in order to receive important information from the DEA, such as registration renewal notices.

  4. Copyright © 2016 Food Safety and Drug Administration Department, Government of Uttar Pradesh, India. All Rights Reserved. Go to Navigation This website uses Javascript

  5. 29 Σεπ 2024 · Last Updated on September 29, 2024. This page list down all the applicable forms, checklists and templates used for registration, renewal, variations, and other regulatory aspects of various types of therapeutic goods. These are categorized according to their applicability under following sections. Human Drugs.

  6. Make changes to drug code, schedule, name, email or address (address change requires approved state license for the new address first) Online Pharmacy Modifications. Modify your existing Retail Online Pharmacy information. Registrant Validation Toolset

  7. www.cdscoonline.gov.in › CDSCO › homepageCDSCO

    CDSCO. Applicants can apply online on SUGAM Portal for Permission to Manufacture , Import or to conduct Clinical Trials as per new Clinical Trial rules of Drugs & Cosmetics Act. Online process for Biologicals (Vaccines & r-DNA) is available on SUGAM.

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