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Regulating Clinical Trials

The Food Safety and Standards Authority of India (hereinafter known as "FSSAI"), which is the apex body for regulating food-based trade in the country had released the Food Safety...

The Food Safety and Standards Authority of India (FSSAI) has issued a new advisory mandating food manufacturers, repackers, and importers to submit quarterly reports on expired and rejected food items via the FoSCoS system.

In a recent move to ensure food safety and quality, the Food Safety and Standards Authority of India (FSSAI) has issued a notification...

In a move seen to tighten regulatory compliance in the food sector, the Food Safety and Standards Authority of India (FSSAI) has mandated the submission of closure reports for all food...

The Food Safety and Standards Authority of India has taken a significant step in fortifying the country’s food safety architecture by notifying the Food Safety and Standards (Contaminants, Toxins and Residues)...

While COVID-19 has brought global and national healthcare under scrutiny, the world continues to depend on Indian pharmaceutical and vaccine manufacturers substantially for their supply of medications.

In a widely shared judgment delivered on August 27, 2025, the Punjab and Haryana High Court, in India, addressed a critical yet often overlooked issue in the Indian healthcare system—doctors' handwriting.

Impact of ENDS on Public Health ENDS or e-cigarettes are battery operated smoking devices.

The Food Safety and Standards Authority of India (FSSAI) in an order dated June 8, 2021, (Order) has mandated that the food businesses shall, be required to declare the registered 14 digit FSSAI...

The regulatory and quality control provisions for the manufacturing of Ayurvedic, Siddha and Unani drugs/ medicines, under the Drugs and Cosmetics Act, 1940, has expedited the process for granting the license.

On 25 July 2025 the Food Safety and Standards Authority of India has issued and advisory that requires every restaurant, café, dhaba and cloud kitchen that the familiar...

On March 28, 2019, the central government has amended the conditions for supply of sublingual tablets of Buprenorphine + Naloxone FDC and Buprenorphine alone.

On January 28, 2020, National Pharmaceutical Pricing Authority (NPPA) fixed the pricing of 17 formulations under Drugs Prices Control Order (DPCO) 2013.

On 9th March 2026, the Ministry of Health and Family Welfare, Government of India, published a significant draft amendment to the Drugs Rules, 1945, by way of Gazette Notification G.S.R. 164(E).

The Central Drugs Standard Control Organization (CDSCO), New Delhi, under the aegis of the Ministry of Health ...

On January 29, 2020, the Union Cabinet approved the Medical Termination of Pregnancy (Amendment) Bill, 2020, to amend the Medical Termination of Pregnancy Act, 1971.