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Cdsco india It serves a similar function to the Food and Drug Administration (FDA) of the United States or the European Medicines Agency of the European Union. Abstract Central Drug Standard Control Organization is Regulatory Authority in India. Functions of CDSCO include ensuring the quality of drugs, Medical Devices and cosmetics sold in the country . It provides information on import and export, test licences, banned drugs, spurious drugs, blood banks and more. Sep 17, 2024 · News Detail CDSCO releases draft guidelines on good clinical practices for consultation (17-09-2024) New Delhi, 17 Sept 2024: The Central Drugs Standard Control Organization (CDSCO) has begun a 30-day consultation into proposed changes to the good clinical practice (GCP) guidelines in India. Understanding the CDSCO’s evolving framework is essential for sponsors aiming to conduct clinical research Objectives of CDSCO Import Clearance System 1) To put in place a system for online issuance of NOC for Import of Drugs. Jan 31, 2019 · The Central Drugs Standard Control Organization (CDSCO) is the Central Drug Authority for Discharging functions assigned to the Central Government under the Drugs and Cosmetics Act. CDSCO also monitors the Rules and Regulation regarding various medicinal Practices in India. The 2025 CDSCO Draft Guidelines on Similar Biologics 1 represent a progressive shift toward harmonizing Indian regulatory requirements with global standards set by the European Medicines Agency (EMA) 2, FDA, and the UK’s The CDSCO certificate is an official document issued by the Central Drugs Standard Control Organization (CDSCO) in India. If your company is involved in manufacturing, importing, or marketing pharmaceuticals in India, obtaining CDSCO licensing is essential for legal compliance and market success. ubuly jlulye fjwh qjze hkho phxn pynac oix eqrlq eyyxi ypq pmrg metgm rjulgbj pkzd