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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 Department of Pharmaceuticals has invited proposals under the CFMDC scheme to strengthen shared testing infrastructure for medical devices, including cardiac and orthopaedic implants, infusion pumps, endoscopic systems, imaging equipment such as X-ray and MRI, and Class B, C, and D IVDs. The initiative aims to improve access to common testing facilities in India.
Source: h7.cl/1hMz2

2. The Department of Pharmaceuticals (DoP) has issued a public notice proposing the inclusion of 11 additional pharmaceutical formulations, including patented biologics and proprietary insulin products, under the Global Tender Enquiry (GTE) exemption list for FY 2025–26. Domestic manufacturers have been invited to submit objections by January 19, 2026, in the attached form.
Source: h7.cl/1hMz7

3. The Supreme Court of India has issued notices to the Union Ministries of Law, Health and AYUSH on a PIL seeking to declare AYUSH practitioners as Registered Medical Practitioners (RMP) under the Drugs & Magic Remedies (Objectionable Advertisements) Act, 1954. An RMP is allowed to display a signboard or notice on their clinic premises indicating that they provide treatment for diseases listed in the Act, which others are prohibited from advertising.
Source: h7.cl/1hMz8

4. Delhi High Court held that in patent disputes involving life-saving drugs, courts must prioritise public interest. Injunctions should not block patient access unless infringement is clearly established through product-to-claim mapping. Where issues are technical and triable, alternative safeguards can protect patentees without withdrawing essential therapies during litigation.
Source: h7.cl/1mK20

5. Indian importers of aluminium beverage cans are reportedly requesting the government to extend the deadline for BIS certification and marking requirements. This follows shortages caused by rising demand and delays in BIS approvals. The quality control order was issued in April 2025, beverage companies have increased imports from West Asia and Sri Lanka to prevent supply disruptions.
Source: h7.cl/1hMzd

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. The Central Consumer Protection Authority (CCPA) has directed all e-commerce platforms to conduct self-audits within three months to eliminate ‘dark patterns’. Platforms are encouraged to submit self-declarations affirming compliance with the 2023 Guidelines for Prevention and Regulation of Dark Patterns.
Source: bit.ly/43SkWPg

2. Indian Government is reportedly planning to introduce a Minimum Import Price (MIP) on pharmaceutical raw materials including Key Starting Materials (KSMs), drug intermediates, and Active Pharmaceutical Ingredients (APIs) to curb the influx of low-cost Chinese imports and support domestic manufacturers.
Source: bit.ly/3Tjvdz6

3. The Ministry of Agriculture and Farmers Welfare has notified the draft Insecticides (Amendment) Rules, 2025, aimed at simplifying licences for insecticides used for household purposes. The amendments reduce application timelines from 90 to 30 days, mandate QR codes on retail packs, and applicants applying for renewal must now meet the educational qualification requirement and require applicants renewing their licences to meet the prescribed educational qualifications.
Source: bit.ly/43PCD23

4. India’s National Consumer Disputes Redressal Commission upheld LIC’s appeal, affirming that insurance contracts require utmost good faith (uberrimae fidei) and placing the burden of disclosure on the insured. Citing the insured’s failure to disclose a prior medical condition as material, it found the State Commission’s award flawed and ordered a fresh review.
Source: bit.ly/3SHoBKU

5. India’s Ministry of Finance has revised several General Financial Rules (GFRs) to ease and expedite procurement processes for scientific equipment and consumables in government-funded research and S&T institutions, by raising financial limits for direct purchases and tenders by head of institutes.
Source: bit.ly/3Zlo8lo