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Drugs Inspector randomly draws drug samples from supply chain for quality checks: Minister

Ruchika SharmaWritten by Ruchika Sharma Published On 2025-04-02T16:41:55+05:30  |  Updated On 2 April 2025 4:41 PM IST
Siflon Drugs and Pharma under scrutiny after Telangana DCA raid uncovers unlicensed drug production
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New Delhi: Drugs Inspector randomly draws drug samples from the supply chain for quality checks under the Drug and Cosmetics Act 1940, the Union Minister of State for Health and Family Welfare, Smt. Anupriya Patel stated.

In a written response to the Rajya Sabha, the Minister stated that list of drugs of various companies, which are declared Not of Standard Quality/ Spurious/ Misbranded/ Adulterated by the Central Drugs Testing Laboratories are regularly uploaded on the website of Central Drugs Standard Control Organization (CDSCO) under the heading of Drug Alert.

An online portal, SUGAM labs has been in place since September 2023 for integrating the drug testing labs of the CDSCO. It automates the entire workflow for testing of Medical Products (Drugs, Vaccine, Cosmetics & Medical devices) to meet the quality specification and tracing the testing status in the laboratories, Patel stated.

Patel emphasized that manufacturers are required to comply with the conditions of the Licence granted under the said Act and Rules to manufacture any drugs for sale and distribution in the country. In case of drug samples declared as Not of Standard Quality by the Drugs Testing laboratories under CDSCO, the respective manufacturing firms are asked for immediate recall and stop further distribution of the Not of standard quality Drugs in the market,

The Minister also said that one of the conditions for licensing is regarding withdrawal/recall/take back of drugs which is reproduced below:

“the licensee shall on being informed by the Licensing Authority or the Controlling Authority that any part of any batch of the drug has been found by the Licensing Authority or the Controlling Authority not to conform with the standards of strength, quality or purity specified in these rules and on being directed so to do, withdraw the remainder of the batch from sale, and, so far as may in the particular circumstances of the case be practicable, recall all issues already made from that batch.”

CDSCOCentral Drugs Testing Labsdrug alertSUGAM labs
Ruchika Sharma
Ruchika Sharma

    Ruchika Sharma joined Medical Dialogue as an Correspondent for the Business Section in 2019. She covers all the updates in the Pharmaceutical field, Policy, Insurance, Business Healthcare, Medical News, Health News, Pharma News, Healthcare and Investment. She has completed her B.Com from Delhi University and then pursued postgraduation in M.Com. She can be contacted at editorial@medicaldialogues.in Contact no. 011-43720751

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