India: Food, Drugs, Healthcare, Life Sciences

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Welcome to the Mondaq Food, Drugs, Healthcare, Life Sciences homepage, here you will find thought leadership articles, podcasts, videos and webinars providing insights covering topics such as Food and Drugs Law, Healthcare, Life Sciences, Biotechnology and Nanotechnology.
Article
When The Cure Becomes The Threat: India’s Proposed Move To Ban Two Antibiotic Families In Animal Medicine
Few public health problems are as quietly dangerous as antimicrobial resistance. It builds slowly, out of sight, in farms and feedlots as much as in hospitals, until the medicines that once saved lives begin to fail. On 3 September 2026, the Ministry of Health and Family Welfare took a notable step against this slow-motion crisis, issuing a draft notification that proposes to prohibit the import, manufacture, sale, and distribution of two specific groups of antibiotics intended for use in animals.
India Healthcare
IL
IndiaLaw LLP
Article
From Food Safety To Due Process: Judicial Scrutiny Of Recent FSSAI Raids In Maharashtra
The recent spate of inspections and raids conducted by the Food and Drug Administration (FDA) and the Food Safety and Standards Authority of India (FSSAI) across Maharashtra has triggered a wider debate on the balance between regulatory enforcement and procedural fairness. Several prominent restaurants, hotels and food establishments found themselves facing suspension orders, stop-business notices and threats of closure allegedly on account of hygiene discrepancies and alleged violations of food safety norms.
India Healthcare
KS
King, Stubb & Kasiva
Article
Energy Drinks, Aged Rum And “100% Pure”: Inside Fssai’s Enforcement Summer
On 7 August 2026, the Delhi High Court stayed an order of the Food Safety and Standards Authority of India (“FSSAI”) prohibiting Dabur India Limited from selling certain food products carrying claims such as “100% Pure”, “100% Natural” and “100% Organic”. Hon’ble Justice Amit Mahajan (Delhi High Court) held that the prohibition ought not to have been passed without an opportunity of hearing. That order captures the season. In recent weeks, the regulator has intensified its enforcement measures to ensure compliance with the Food Safety and Standards Act, 2006, and the courts have begun to ask how far it may go.
India Healthcare
SA
Sarthak Advocates & Solicitors
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Article
Indian FSSAI’s New Labelling Rules 2026
India's food safety regulator has introduced new labelling amendments that simplify compliance for infant nutrition products and small packages while strengthening traceability requirements for non-retail containers. Meanwhile, the Supreme Court is pushing for front-of-pack warning labels on products high in fat, sugar, and salt, raising critical questions about implementation thresholds, consumer accessibility, and the balance between public health and industry concerns.
India Consumer
GA
Global Advertising Lawyers Alliance (GALA)
Article
Indian FSSAI’s Aug’26 Enforcement Wave — What Food And Beverage Advertisers Should Know
India's Food Safety and Standards Authority intensified enforcement in August 2026, targeting major food and beverage companies over "100%" purity claims, energy drink labeling, and packaging compliance. The regulatory actions against Dabur, ITC, Diageo, and over 150 other companies reveal how product names, packaging, and advertising copy are now treated as interconnected consumer protection issues requiring coordinated legal review.
India Consumer
GA
Global Advertising Lawyers Alliance (GALA)
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Article
Life Sciences And Healthcare Newsletter | July 2026
India's life sciences regulatory landscape in July 2026 saw major developments across pharmaceuticals, medical devices, and healthcare regulation. Key changes included the draft National Pharmacy Commission Bill proposing to replace the 80-year-old Pharmacy Act, CDSCO's final guidance on Medical Device Software establishing clear market access pathways, and stricter controls on high-alcohol oral formulations under Schedule H1.
India Healthcare
DL
Dentons Link Legal
Article
Medical Devices Rules: Faster Manufacturing Licence Approvals
The Union Ministry of Health and Family Welfare (the “Ministry”) has recently published a Draft Notification[1] in the Official Gazette proposing amendments to the Medical Devices Rules, 2017[2] (the “Rules”), promulgated under the Drugs and Cosmetics Act, 1940. The proposed amendments specifically target the statutory timelines prescribed for processing manufacturing licence applications across the four risk-based classifications of medical devices.
India Healthcare
SR
S.S. Rana & Co. Advocates
Article
USPTO Streamlined Claim Set Pilot Program: A Strategic Pathway To Accelerated Patent Examination
Patent pendency remains one of the most significant challenges in U.S. patent prosecution. Average first-action wait times range from approximately 20 to 29 months across Technology Centers, creating real costs for startups seeking investor credibility, life sciences companies racing toward product launches, and technology firms defending competitive market position.
India IP
SR
S.S. Rana & Co. Advocates
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Article
Data Protection Laws For Healthcare Companies And Hospitals
Healthcare organisations in India handle highly sensitive patient information, from medical histories to genetic data. With the Digital Personal Data Protection Act, 2023 and new DPDP Rules, 2025 creating a modern statutory framework, hospitals and healthcare companies must navigate complex requirements around lawful data collection, secure storage, patient rights, vendor governance, and incident response while balancing clinical operations with evolving privacy obligations.
India Privacy
MH
Mansukhlal Hiralal & Co.
Article
When The Cure Becomes The Threat: India’s Proposed Move To Ban Two Antibiotic Families In Animal Medicine
Few public health problems are as quietly dangerous as antimicrobial resistance. It builds slowly, out of sight, in farms and feedlots as much as in hospitals, until the medicines that once saved lives begin to fail. On 3 September 2026, the Ministry of Health and Family Welfare took a notable step against this slow-motion crisis, issuing a draft notification that proposes to prohibit the import, manufacture, sale, and distribution of two specific groups of antibiotics intended for use in animals.
India Healthcare
IL
IndiaLaw LLP
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