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  • Over 36 percent of...

Over 36 percent of inspected drug-making units had to be shut: CDSCO chief

Written By : Ruchika Sharma |Medically Reviewed By : Dr. Kamal Kant Kohli Published On 2024-06-29T14:30:11+05:30  |  Updated On 6 Aug 2024 12:52 AM IST
Counterfeit versions of Montek-LC Tablets seized in Telangana
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"The issues in the Indian pharma industry relate to "non-compliance which leads to quality issues," CDSCO Chief

Bengaluru: India's drug regulator reported that over 36 percent of the 400 drug manufacturing units inspected since last year have been directed to close. This action follows heightened scrutiny prompted by deaths associated with sub-standard cough syrups.

India, known as a global pharmaceutical hub due to its vast drug production, is actively working to rebuild trust after Indian-manufactured cough syrups were implicated in child deaths in Gambia, Uzbekistan, and Cameroon.

According to a Reuters report, India's Central Drugs Standard Control Organization (CDSCO) chief Rajeev Raghuvanshi said that after one and a half years of inspections, he was "not very happy to say that more than 36 per cent of them (manufacturing units) had to be closed."
The issues in the Indian pharma industry relate to "non-compliance which leads to quality issues," he told an event in Mumbai.
He did not elaborate or name any companies.
Cough syrups made in India and Indonesia have been linked to the deaths of more than 300 children globally. The medicines were found to contain high levels of two known toxins, diethylene glycol and ethylene glycol, leading to acute kidney injury and death.
India is the world's third largest maker of drugs by volume after the United States and China. India's pharma export sales are expected to reach $55 billion by 2030, according a government-backed trade body Pharmaceuticals Export Promotion Council of India (Pharmexcil). Export sales in 2023-2024 were $27.85 billion.
Prime Minister Narendra Modi's government late last year also issued revised guidelines to ensure compliance with global standards and made it mandatory for all of country's drug manufacturing units to adhere to them.
"We have not had any complaint from World Health Organization (WHO) or any other agency since last July .. we've been able to control the issues that were happening from a quality point of view," Raghuvanshi said.

Read also: Maiden Pharma denies tampering with tests in probe of cough syrup deaths

cough syrupCDSCORajeev Raghuvanshi
Source : with inputs
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

    Dr. Kamal Kant Kohli
    Dr. Kamal Kant Kohli

    Dr Kamal Kant Kohli-MBBS, DTCD- a chest specialist with more than 30 years of practice and a flair for writing clinical articles, Dr Kamal Kant Kohli joined Medical Dialogues as a Chief Editor of Medical News. Besides writing articles, as an editor, he proofreads and verifies all the medical content published on Medical Dialogues including those coming from journals, studies,medical conferences,guidelines etc. Email: drkohli@medicaldialogues.in. Contact no. 011-43720751

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