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  • Draft Guidance on The Quality and Clinical Requirements for Inhalation and Nasal Medicinal Products

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    Posted On: Oct 04, 2023

  • Draft Guidelines for Listing of Tobacco Products

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    Posted On: Oct 04, 2023

  • Intention for Cancellation of Products with Pending Retention Fees

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    Posted On: Jul 26, 2023

  • Draft Guidelines for Handling Unfit Medical Devices and Diagnostics

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    Posted On: Jul 19, 2023

  • The Use of Antimicrobial Preservatives in Oral Solid Dosage Formulations

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    Posted On: Jun 21, 2023

  • New Guidelines for Good Manufacturing Practices (GMP) Inspection of Human Medicinal Products Manufacturing Facilities, 2023

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    Posted On: Jun 16, 2023

  • Request for EOI for Shortlisting of Evaluators

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    Posted On: Jun 09, 2023

  • Publication of Clinical Trial Public Assessment Reports and GCP Public Inspection Reports

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    Posted On: Jun 02, 2023

  • Timelines for Issuance of Clinical Trial Certificates

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    Posted On: May 29, 2023

  • Training on Good Regulatory Practices for Stakeholders and Dealers in Medical Devices, Diagnostics and Laboratory Equipment

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    Posted On: Apr 08, 2023