cdsco Rigitration

A drug license is essential for the legal operation of businesses involved in the manufacturing, distribution, and sale of pharmaceuticals and related products.




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Required Documents

  • Application Form
  • Proof of Identity and Address
  • Business Details
  • Proof of Premises
  • Site Plan/Layout
  • Equipment and Facilities
  • Qualified Personnel
  • Standard Operating Procedures (SOPS)
  • No Objection Certificate (NOC)
  • Bank Details
  • Affidavit/Declaration
  • Benefits of CMDSCO

    Legal Compliance:

    It is mandatory under Indian law for anyone involved in the manufacture, sale, or distribution of drugs. Operating without a valid license is illegal and can result in severe penalties, including fines and imprisonment.

    Operational Legitimacy

    Provides legitimacy to your business operations and helps in gaining trust from customers, suppliers, and other stakeholders.

    Business Expansion

    A valid drug license can facilitate business growth, including expanding into new regions or product lines, as it demonstrates regulatory compliance.

    Avoiding Legal Issues

    Prevents legal complications and interruptions in business operations by ensuring adherence to drug laws and regulations.

    FAQ

    CDSCO stands for the Central Drugs Standard Control Organization. It is the national regulatory body for overseeing the quality, safety, and efficacy of drugs and medical devices in India.

    CDSCO is responsible for: - Granting licenses for manufacturing and selling drugs. - Approving new drugs and clinical trials. - Regulating the import of drugs and medical devices. - Ensuring drug quality and safety through inspections and enforcement.

    To apply for a drug license, visit the CDSCO website and follow the guidelines provided in the online application system. You will need to provide necessary documents and details about the manufacturing or trading entity.

    - Application form (Form 27 for manufacturing or Form 28 for selling) - Proof of identity and address of the applicant - Manufacturing or business premises details - Details of technical staff and their qualifications - Certificate of good manufacturing practices (GMP)

    You can check the status of your application on the CDSCO online portal. You will need to log in with your credentials and navigate to the application status section.

    ADRs can be reported through the CDSCO’s Pharmacovigilance Programme. You can submit reports online via the CDSCO portal or contact the nearest CDSCO office for guidance.

    To import drugs or medical devices, you need to apply for an import license from CDSCO. You will have to provide: - Importer’s license - Details of the drug or device - Certificate of analysis - Proof of compliance with Indian standards

    If you lose your DSC, report it immediately to the Certifying Authority to revoke it and apply for a new one.

    If you wish to appeal a decision made by CDSCO, you should follow the formal procedure outlined on the CDSCO website. This typically involves submitting a written appeal with supporting documents to the appropriate CDSCO authority.

    Yes, CDSCO charges fees for various services, including licensing, registration, and approvals. The fee structure is available on the CDSCO website and is subject to change.

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