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TOP 5 HEALTH LAWS AND POLICY UPDATES

Dear Readers, we are happy to share the most interesting legal and policy updates concerning health industry that we read today. we hope you enjoy reading it.

1. The Supreme Court of India by dismissing a review petition held that doctors and medical professionals rendering paid services will fall under the Consumer Protection Act 1986.
Source: bit.ly/3EJukMp

2. The Department of Telecommunications (DoT) has directed social media and application hosting platforms to remove content enabling Caller ID spoofing, citing violations of the Telecommunications Act, 2023. The advisory warns that tampering with telecom identifiers is a cognizable and non-bailable offence, and platforms failing to comply may face legal action.
Source: bit.ly/4k8UNDu

3. The Indian Pharmaceutical Association (IPA) has raised serious concerns over the National Pharmaceutical Pricing Authority (NPPA) mandate for all offline and online pharmacies to display current drug prices on their websites to protect consumers from overpaying as impractical and unfeasible.
Source: bit.ly/4k3GEY3

4. The WHO’s 2025 update to the International Classification of Diseases (ICD-11) introduces a new module for traditional medicine, recognizing Ayurveda, Siddha, and Unani systems alongside conventional healthcare. This move strengthens their role in global health reporting, research, and policymaking, fostering integrative healthcare.
Source: bit.ly/4kagsv4

5. The Food Safety and Standards Authority of India (FSSAI) has proposed a draft amendment to the Food Safety and Standards (Labelling and Display) Regulations, 2020. Key changes include mandatory bold labeling of added sugar, saturated fat, and sodium content, a compulsory logo as provided on all milk and milk products, and clearer front-of-pack declarations for coffee-chicory mixtures. Public objections or suggestions can be submitted within 60 days from the date issuance of notification.
Source: bit.ly/40Zx4ws

Posted on

TOP 5 HEALTH LAWS AND POLICY UPDATES

Dear Readers, we are happy to share the most interesting legal and policy updates concerning health industry that we read today. We hope you enjoy reading it.

1. India’s Ministry of Environment, Forest, and Climate Change has released draft rules under the Environment Protection Act, 1986, proposing Extended Producer Responsibility (EPR) for managing post-consumer waste from paper, glass and metal packaging along with sanitary products. These Rules aim to promote recycling, reuse, and waste-to-energy initiatives. Producers, importers, and brand owners must register and meet EPR targets from April 2026.
Source: bit.ly/49w0GFK

2. India’s Central Pollution Control Board (CPCB) has regulated the micro and small importers, producers, sellers and manufacturers of plastic raw materials and have mandated their registration on the EPR Plastic Portal. Filing of annual returns and compliance with all other EPR obligations is also outlined in the guidance issued by CPCB.
Source: bit.ly/49CJo9Z

3. India’s Supreme Court has reiterated that Ayurvedic/AYUSH doctors cannot claim parity with allopathic doctors, citing differences in academic qualifications and the standards of their respective courses. The court dismissed a petition by AYUSH doctors in Kerala, referring to past judgments that clarified the distinction in responsibilities and remuneration between allopathic and AYUSH practitioners.
Source: bit.ly/4iqyYhN

4. India’s Delhi District Consumer Commission has fined a leading FMCG company with a fine of ₹15 lakh for misleading advertisements about its “Fair and Handsome” cream, which claimed to provide fairness within three weeks without proper evidence. The Commission found the claims deceptive and an unfair trade practice, ordering the company to withdraw all misleading ads and packaging.
Source: bit.ly/3OPcMjE

5. India’s Central Drugs Standard Control Organization (CDSCO) has issued a circular thereby directing all State and Union Territory Drugs Controllers to ensure the approval of drugs and medical devices for rare diseases within 90 days of receiving applications to expedite the regulatory process and support faster access to treatment for rare diseases.
Source: bit.ly/3VvSFLl