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Medicines Health Regulatory Authority

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WHO issues alert against Indian cough syrups. They are...

The World Health Organisation has issued an alert against three "substandard" oral cough syrups identified in India -- Coldrif, Respifresh TR and ReLife -- and urged national regulatory authorities......

Alerted Centre, MP govt about toxic cough syrup: TN minister

The Tamil Nadu government had alerted the Madhya Pradesh government and the Union Health Ministry about the presence of a toxic substance in Coldrif cough syrup, besides notifying authorities in......

Where The Deadly Cough Syrup Was Made

Sandwiched between a Hero MotoCorp showroom and a shop that hires out cooking utensils is a small, dingy building that's been locked up.The non-descript two-room building is a manufacturing unit of......

Cough syrup deaths: IMA slams doctor's arrest

The Indian Medical Association (IMA) has come out in defence of a doctor arrested in connection with cough syrup deaths in Madhya Pradesh, saying the approval of the syrup and monitoring its......

3 cough syrups have been recalled: India replies to WHO

Central drug regulator Central Drugs Standard Control Organisation (CDSCO) has informed the World Health Organisation (WHO) that three cough syrups -- Coldrif, RespifreshTR and ReLife -- have been......

Tylenol row may not hit India's pharma exports

Amid controversy over USPre­sident Donald Trump’s comm­ents linking the use of Tylenol and other related paracetamol products by pregnant women to autism in children, experts and industry......

Herbal drug cos to swallow bitter European pills

UK health regulatory authority enforces strict norms for export, in wake of EU directive. Indian ayurvedic medicines manufacturers are set to face a tough time as far as exports to European......

USTR flags hurdles in medical device exports to India

The USTR report, released just ahead of the US' April 2 deadline for implementing reciprocal tariffs, has also cited high tariffs and price caps, which have not increased in line with inflation, as......

GSK withdraws sale of Zinetac after health alert

GSK is continuing with investigations into the potential source of the NDMA, which is a known environmental contaminant and found in water and foods, including meats, dairy products, and......

What is Schedule M and why it's mandatory for all pharma units

With an eye on improving quality assurance in the wake of increased global scrutiny on Indian pharma products, the Centre on Tuesday said that Schedule M of the Drugs and Cosmetics Act, 1940 will......

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