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AstraZeneca reaffirms Covid vaccine safety amid rare TTS concerns

In light of recent concerns surrounding potential rare side effects of the AstraZeneca-Oxford COVID-19 vaccine, the pharmaceutical giant has reiterated its commitment to patient safety while......

AstraZeneca admits in court: Covishield causes TTS

United Kingdom-headquartered pharmaceutical giant AstraZeneca (AZ) has admitted that in 'very rare cases' its Covid vaccine can cause a blood clot related side effect but the causal link is......

Oxford-AstraZeneca Covid jab faces legal threat in UK over side effects: Report

The Oxford-AstraZeneca COVID-19 vaccine, known as Vaxzevria in Europe and licensed as Covishield in India, is facing a legal challenge in the high court in London, a UK media report said on......

Serum Institute gets nod to resume vaccine trial in India

Drugs Controller General of India Dr V G Somani on Tuesday gave permission to Serum Institute of India to resume clinical trial of the Oxford COVID-19 vaccine candidate in the country while......

Serum Inst to resume Covid vaccine trials after DCGI nod

Serum Institute of India will resume clinical trials of AstraZeneca's COVID-19 vaccine candidate after getting the permission from the Drugs Controller General of India (DCGI), the Pune-based......

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......

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......

Indian pharma cos get a shot in the arm in $12-bn Australian drug market

Indian drug firms get a shot in the arm in the $12 bn Australian drug market as the Therapeutic Goods Administration (TGA), Australia agrees to accelerate the drug approval process in that country......

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......

Regulator asks traders to stock 55 ICU drugs

This is apart from the requirement to stock hydroxychloroquine (200 mg) and Azithromycin (500 mg) tablets for patients requiring ICU management, asymptomatic healthcare workers and asymptomatic......

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Medicines Health Regulatory Authority

News for Medicines Health Regulatory Authority

AstraZeneca reaffirms Covid vaccine safety amid rare TTS concerns

AstraZeneca admits in court: Covishield causes TTS

Oxford-AstraZeneca Covid jab faces legal threat in UK over side effects: Report

Serum Institute gets nod to resume vaccine trial in India

Serum Inst to resume Covid vaccine trials after DCGI nod

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

Herbal drug cos to swallow bitter European pills

Indian pharma cos get a shot in the arm in $12-bn Australian drug market

GSK withdraws sale of Zinetac after health alert

Regulator asks traders to stock 55 ICU drugs

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