High out-of-pocket expenditure remains the main barrier to Universal Health Coverage for diseases like cancer. Evaluate recent regulatory and fiscal measures to address it.
New · District CollectorCan you hold the district for 72 hours?Floods, a heatwave, an outbreak, a grievance queue. Take the decisions, see the consequences.Play →Cancer treatment pushes many Indian households into catastrophic out-of-pocket expenditure (OOPE). A key driver is the supply-chain mark-up on drugs, which NPPA found averaged ~170% and reached 700%+ in some cases [1]. Recent measures have made real gains, but these remain incomplete.
Regulatory measures: gains
- Trade Margin Rationalisation (TMR): In 2019, NPPA used Para 19, DPCO 2013 to cap margins at 30% on 42 non-scheduled cancer drugs. MRPs of 526 brands fell ~50% on average, saving patients ~₹984 crore a year [2].
- 2026 extension: The 30% cap now covers all non-scheduled anti-cancer drugs: branded or generic, patented or imported. Prices are expected to fall up to 70%, saving ₹2,500 crore a year. Manufacturers must keep production at current levels [1].
- Cooperative federalism: Maharashtra, Rajasthan and Karnataka pressed for the cap [1].
Fiscal measures: gains
- Budget 2025-26: 36 life-saving drugs are fully exempt from Basic Customs Duty and 6 attract a concessional 5%. Drugs supplied under Patient Assistance Programmes are also exempt [3].
- Day Care Cancer Centres will be set up in all district hospitals within three years (200 in 2025-26), cutting travel and indirect costs [4].
Limitations
- Weak legal footing: DPCO allows margin capping only temporarily. The Standing Committee on Chemicals and Fertilisers urged amending DPCO [5]. In 2026 it again flagged the absence of a permanent TMR framework [6].
- Enforcement gaps: Price-to-stockist data is not public, so patients cannot check margins [5]. Large overcharged amounts are stuck in litigation, and NPPA lacks hospital and rural sales data [6].
- Design flaw: A flat 30% margin is largest in rupee terms on the costliest drugs. WHO advises regressive mark-ups instead (lower rates for higher-priced drugs) [7]. The manufacturer's price, the main cost of patented imports, remains free [1].
- Availability risk: The supply condition binds only manufacturers. Chemists in small towns may stop stocking low-margin specialty drugs.
Overall, margin caps and duty relief have substantially reduced the price of cancer drugs. The way forward is to:
- put TMR into DPCO through a statutory amendment;
- disclose PTS data;
- adopt a WHO-style regressive mark-up;
- track drug availability in district markets.
Combined with decentralised care, these steps can turn lower prices into lower OOPE. That would bring India closer to SDG 3.8: universal health coverage with financial protection.
Sources
- 1PIB: Government Expands Cancer Medicine Price Controls; Cancer Patients Expected to Save ₹2,500 Crore Annually (Oct 2026)170%/700% mark-ups, 30% cap on all non-scheduled anti-cancer drugs, up to 70% price fall, ₹2,500 crore savings, production condition, State demands, manufacturer price uncontrolled
- 2PIB: NPPA has put a cap on Trade Margin of 42 select non-scheduled anti-cancer medicines under TMR ApproachPara 19 use, 526 brands, ~50% average cut, ₹984 crore savings
- 3PIB: Union Budget 2025-26 proposes to remove seven customs tariff rates for industrial goodsBCD exemption for 36 drugs, 5% on 6, Patient Assistance Programme exemptions
- 4PIB: Towards a Cancer-Free India (Feb 2025)Day Care Cancer Centres in all district hospitals, 200 in 2025-26
- 5PRS Legislative Research: Price Rise of Medicines in the Pharmaceutical Sector (Standing Committee report summary)TMR only temporary under DPCO, amendment recommended, PTS data not public
- 6PRS Legislative Research: Monthly Policy Review, August 2026no permanent TMR framework, unrecovered overcharging in litigation, NPPA data gaps
- 7WHO Guideline on Country Pharmaceutical Pricing Policies (2020)recommends regressive rather than fixed-percentage mark-ups
Practice
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