Revised MRPs of 1,364 Anti-Cancer Formulations Come into Effect from Today
FlashcardsQuick reviseKey facts. One by one.Start →In this note
- At a Glance
- Why in the News
- Background & Evolution
- Core Static Facts
- Multi-Dimensional Analysis
- Recent Developments (last 12-18 months)
- Prelims Hooks (high-density factual bullets)
- The Cap Cuts the Trader's Share, Not the Company's Price
- How to Read the ₹3,540 Crore Savings Figure
- A Temporary Power Doing a Permanent Job
- Why Catching an Overcharger Is Easier Than Getting the Money Back
- Could a Percentage Cap Push Cheaper Brands Off the Shelf?
- The Cap Reaches the Bills That Insurance Leaves Out
- Anchors for Answers
- Mains Relevance
- Related Topics to Study Next
- NCERT Concepts to Revise
- Common Errors / Trap Areas
1. At a Glance
- NPPA capped the trade margin on 137 non-scheduled anti-cancer drugs at 30% of MRP, using its special power under Para 19, DPCO 2013. Revised MRPs took effect on 9 November 2026 [1][2].
- As on 8 November 2026, 85 companies had reported revised MRPs for 1,364 formulations covering 121 drugs. Expected consumer savings are ₹3,540.38 crore a year [1].
- It scales up the 2019 pilot of 42 drugs, which PIB described as a proof of concept [3].
- UPSC value: it links health affordability, drug-price regulation, inter-ministerial division of work and consumer-driven enforcement.
2. Why in the News
- 17 Oct 2026: Gazette notification capped trade margins on 137 anti-cancer drugs [2].
- 28 Oct 2026: NPPA released revised MRPs for an initial 543 brands, with the list to be updated continually [6].
- 8 Nov 2026: Reported position reached 1,364 formulations, 121 drugs and 85 companies. 679 brands reported cuts above 50%, and the highest cut was 96.45% [1].
- 9 Nov 2026: Revised MRPs came into force [1][2].
3. Background & Evolution
- Pre-2013: NPPA fixed prices under the DPCO 1995 formula [13].
- DPCO 2013: The current framework for regulating drug prices in India [10].
- 26 Feb 2019: NPPA invoked extraordinary powers in public interest (Para 19) to bring 42 non-scheduled anti-cancer drugs under Trade Margin Rationalisation (TMR) [4].
- 2019 outcome:
- Trade margin was capped at up to 30% of MRP, and MRPs of 526 brands fell by up to 90% [3].
- An earlier 2019 release reported MRPs of 390 non-scheduled anti-cancer medicines reduced by up to 87% [5].
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Later estimates put savings at about ₹984 crore a year, with about 500 brands reduced by an average of about 50% [11].
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Union Budget 2024-25: Customs duty was removed on three additional cancer medicines [12].
- 2026: TMR expanded to 137 drugs on an Expert Committee's recommendation [1][2].
4. Core Static Facts
| Item | Fact |
|---|---|
| Regulator | NPPA, Department of Pharmaceuticals, Ministry of Chemicals and Fertilizers [1] |
| Expert advice | Committee constituted by DGHS, Ministry of Health & Family Welfare [1] |
| Legal basis | Para 19, DPCO 2013 [2] |
| Cap | 30% of MRP [2] |
| Drugs capped | 137 non-scheduled anti-cancer drugs [2] |
| Examples | Immunotherapy drugs, Denosumab, Pegfilgrastim, Bevacizumab [2] |
| Gazette / effective date | 17 Oct 2026 / 9 Nov 2026 [2] |
| Manufacturer reporting | Within 7 days of publication [2] |
| Reported so far (8 Nov 2026) | 1,364 formulations, 121 drugs, 85 companies [1] |
| Projected MRP cut | Up to 70% [2] |
| Highest reported cut | 96.45% [1] |
| Expected savings | ₹3,540.38 crore a year [1] |
| Price check | MRP on pack, Pharma Sahi Daam app, nppa.gov.in [1] |
| Complaints | Pharma Jan Samadhan portal, NPPA helpline [1] |
| Enforcement | State Drug Controllers; hospitals and medical institutions are responsible for revised prices on direct supplies [2] |
Key distinctions
- Scheduled drugs: NLEM medicines are placed in the First Schedule of DPCO 2013, and NPPA fixes their ceiling prices [9][10].
- This action: It covers non-scheduled drugs through a margin cap, not a formula-based ceiling price [2].
- Trade margin cap vs MRP: The cap is the tool and the revised MRP is the outcome [1].
5. Multi-Dimensional Analysis
Economic
- Savings of ₹3,540.38 crore are about 3.6 times the ₹984 crore estimated for the 42-drug pilot [1][11]. The two are separate estimates, so the ratio is only indicative.
- Cuts of up to 96.45% suggest some products carried very wide margins [1]. This is an inference, not an official finding.
- Analysis: A margin cap targets distribution markups and leaves the drug unchanged, but it may squeeze trade incentives to stock low-priced brands.
Social
- A 2019 PIB release said cancer had the highest out-of-pocket spending of any disease in 2014 [4].
- Studies it cited suggest about 60% of households borrow and about 32% rely on friends and relatives for cancer hospitalisation [4].
- A Tata Memorial–ACTREC study found a 6-month course of some modern drugs can cost more than several years of income in India [8].
Legal / Regulatory
- Para 19 allows intervention beyond the scheduled list, in public interest [4].
- Analysis: Repeated use of an extraordinary power for a whole therapeutic class raises the question of whether TMR needs a standing statutory framework.
Administrative / Federal
- The process crosses ministries: Health advises and NPPA, under Chemicals and Fertilizers, implements [1].
- Enforcement relies on State Drug Controllers, which makes state capacity decisive [2].
- Direct hospital supply is explicitly covered, closing an obvious leakage route [2].
Ethical / Governance
- Public verification and grievance channels shift part of monitoring to consumers [1].
- Analysis: Patients in acute treatment, often buying through hospital pharmacies, are poorly placed to act as enforcers.
Scientific / Technological
- Coverage extends to high-cost modern therapies such as immunotherapy and biologic-type products [2].
- Funds for one pembrolizumab patient in India could treat 18–22 patients on lower-cost targeted therapies, so price cuts alone do not settle allocation [8].
6. Recent Developments (last 12-18 months)
- Mar 2026: Tata Memorial–ACTREC study on unaffordability of modern head and neck cancer drugs [8].
- Oct 2026: PIB release on expanded cancer price controls projected savings of ₹2,500 crore a year [7].
- 17 Oct 2026: Gazette notification on 137 drugs [2].
- 28 Oct 2026: First revised list of 543 brands [6].
- 8 Nov 2026: Reported coverage of 1,364 formulations, with 679 brands cut by more than 50% [1].
- 9 Nov 2026: Revised MRPs effective [1].
7. Prelims Hooks (high-density factual bullets)
- NPPA functions under the Department of Pharmaceuticals, Ministry of Chemicals and Fertilizers [1].
- The Expert Committee was constituted by DGHS, Ministry of Health & Family Welfare [1].
- The 2026 margin cap was imposed under Para 19, DPCO 2013 [2].
- The trade margin cap is 30% of MRP [2].
- The cap covers 137 non-scheduled anti-cancer drugs [2].
- Revised MRPs took effect on 9 November 2026 [1].
- Manufacturers had to report revised prices within 7 days of Gazette publication [2].
- 1,364 formulations of 121 drugs were reported by 85 companies as on 8 November 2026 [1].
- Highest reported MRP reduction: 96.45% [1].
- Expected annual consumer savings: ₹3,540.38 crore [1].
- Pharma Sahi Daam is NPPA's app for checking medicine prices [1].
- Pharma Jan Samadhan is NPPA's portal for overcharging complaints [1].
- The first anti-cancer TMR, in February 2019, covered 42 drugs [4].
- NLEM medicines are incorporated in the First Schedule of DPCO 2013 [9][10].
8. The Cap Cuts the Trader's Share, Not the Company's Price
- The cap controls only one part of the price
- A trade margin is the share of the price kept by wholesalers and retailers.
- Example (not official data): at a 30% cap, if a company sells a drug at ₹70,000, the MRP (maximum retail price) can still be ₹1 lakh.
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So a drug with a very high company price stays very expensive after the cap.
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For new cancer drugs, the company's price is often the main problem
- WHO's 2018 report found that research and production costs may have little link to cancer drug prices [21].
- Companies often set prices by how much a buyer is willing to pay [21].
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A margin cap does not touch this decision.
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The same drug can cost very different amounts in different countries
- For pembrolizumab, a WHO document found prices from $12.23 to $60.98 per mg of API (the active ingredient), about a five-fold gap [24].
- It expects biosimilars (close, cheaper copies of biological drugs) in 3 to 5 years, which could lower prices sharply [24].
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Competition may therefore cut prices of the costliest drugs in ways a margin cap cannot.
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The Department of Pharmaceuticals and the Health Ministry should add a second tool for the costliest drugs
- WHO's guideline asks countries to use several pricing policies together, and not rely on one [22].
- Its list includes tendering (buyers ask companies to bid for a large order) and price transparency [22].
- Tendering pushes down the company's own price, which is the part this cap leaves alone.
9. How to Read the ₹3,540 Crore Savings Figure
- It is an estimate, and it moved quickly
- In October 2026, a PIB release projected savings of ₹2,500 crore a year [7].
- By 8 November, the figure was ₹3,540.38 crore, over ₹1,000 crore higher [1].
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Reports had also covered only 121 of the 137 drugs by then, so the final picture is not yet known [1][2].
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A lower MRP saves money only if the buyer was paying the old MRP
- A patient who already got a large discount saves less than the headline suggests.
- Where a scheme pays the bill, the saving goes first to the scheme and not to the patient.
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This is reasoning, not an official finding. The sources used here do not explain how the figure was calculated.
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A big percentage cut does not mean a big total saving
- The highest cut of 96.45% [1] means a ₹100 MRP fell to about ₹3.55. The old price was about 28 times the new one.
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This shows how high that one MRP was. It does not show how many patients bought that brand.
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Use the figure carefully in an answer
- Write 'expected savings of ₹3,540.38 crore a year' [1], not 'patients have saved'.
10. A Temporary Power Doing a Permanent Job
- Parliament's committees have now named this weakness directly
- A parliamentary committee noted that DPCO 2013 (the Drugs Prices Control Order) permits trade margin capping only for a limited period [16].
- It recommended amending DPCO to allow trade margin rationalisation and to regulate non-scheduled drugs (medicines outside the government's essential list) [16].
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In August 2026, the Standing Committee on Chemicals and Fertilisers (Report No. 33) again flagged the lack of a permanent trade margin framework [15].
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Without a standing rule, protection arrives only when a new order is issued
- The first cancer order came in 2019 and the wider one in 2026 [4][2].
- A cancer drug left out of the 2019 list had no margin cap for those seven years.
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Non-scheduled drugs can raise prices by up to 10% a year [17]. At that rate, a price nearly doubles in seven years.
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Check what happens when the period ends
- If the cap is time-limited and is not renewed, margins can widen again.
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The sources used here do not state how long the 2026 cap lasts, so read the Gazette before writing a date.
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The Department of Pharmaceuticals should write trade margin rules into DPCO itself
- The rule should say when a drug class enters the cap, for how long, and how it is reviewed. The committee's recommendation supports this [15][16].
- The rule should also fix the gaps Report No. 33 found in how scheduled and non-scheduled medicines are classified [15].
11. Why Catching an Overcharger Is Easier Than Getting the Money Back
- Recovery can get stuck in court for years
- When NPPA finds overcharging, it issues a demand notice, an order to repay the excess with interest [19].
- Companies can challenge this in court. In 2011, ₹1,930.41 crore of ₹2,328.53 crore in demand notices was under litigation, about 83% [18].
- In August 2026, the Standing Committee still reported large unrecovered amounts stuck in litigation [15].
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So a company may gain more by delaying than it risks by overcharging.
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Even when money is recovered, the patient may not see it
- A demand notice recovers the excess for the government, and the sources used here describe no route that refunds an individual patient.
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This matters most in cancer care, where the family may already have borrowed to pay [4].
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NPPA cannot show which state is failing
- Enforcement of this order rests on State Drug Controllers [2].
- But NPPA does not keep a state-wise record of overcharging by companies [19].
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Without that record, nobody can compare states or see where checks are weak.
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A low complaint count proves little
- State Price Monitoring and Resource Units and State Drug Controllers refer cases to NPPA [20].
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NPPA told Parliament it received no complaint about loose medicines being sold above per-unit MRP [20]. That shows only what was reported, not what happens in shops.
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NPPA should publish overcharging data by state
- The data should cover cases, amounts and recoveries.
- Report No. 33 has already pointed to incomplete data for price monitoring [15].
12. Could a Percentage Cap Push Cheaper Brands Off the Shelf?
- The strongest objection
- A cap set as a percentage pays the trader more on a costly brand.
- Example (not official data): at 30%, a seller can earn up to ₹3,000 on a ₹10,000 brand but only ₹300 on a ₹1,000 brand.
- So a trader may prefer to stock the costlier brand, or stop stocking cheap ones.
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A WHO South-East Asia review found evidence of unintended, harmful effects from several mark-up policies [23]. A mark-up is the amount added to a price at each step of the supply chain.
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What is right about it
- The incentive is real, because it follows directly from how a percentage works.
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The review warns that a price rule can backfire [23], so a fall in MRP alone does not prove success.
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Where it falls short
- The WHO review covers mark-up policies in the region in general, not India's cancer margin cap.
- The sources used here contain no study showing that the 2019 cancer drugs disappeared from shelves.
- Hospitals are also bound to the revised price on direct supply [2], which limits one way of avoiding the cap.
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So the risk is possible but unproven. An honest answer should say both.
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NPPA should track availability, not only price
- It should publish stock data for the 137 capped drugs from before and after 9 November 2026.
- This would settle the question with evidence, and would also help fix the data gap noted by the Standing Committee [15].
13. The Cap Reaches the Bills That Insurance Leaves Out
- This is the strongest argument in favour of the order
- PM-JAY (the government's health insurance scheme for poorer families) covers only inpatient care, meaning treatment after hospital admission [25].
- The Health Committee called this inadequate, because out-of-pocket spending (money patients pay themselves) is mostly on outpatient care and medicines [25].
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A lower MRP helps in the part of the bill that insurance does not pay.
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But cover and price cuts do not add up to full protection
- PM-JAY gives ₹5 lakh per family per year and defines 435 cancer procedures [26].
- A six-month course of some modern drugs can cost more than several years of income [8].
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Even a large cut may leave such a drug out of reach for a poor family.
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Cheap outlets are few
- AMRIT pharmacies offered 289 cancer medicines through 217 outlets as of June 2025 [27].
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For a patient far from these outlets, the MRP on the pack remains the price that matters.
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The Health Ministry should act on the committee's concern
- It should examine covering outpatient cancer medicines under PM-JAY, since the committee has identified that gap [25].
- Price control lowers the bill. Only insurance or public supply decides who pays what remains.
14. Anchors for Answers
- Data: ₹1,930.41 crore of ₹2,328.53 crore in NPPA demand notices was under litigation in 2011, about 83% [18]
- Data: Pembrolizumab costs from $12.23 to $60.98 per mg of active ingredient across countries [24]
- Data: PM-JAY gives ₹5 lakh per family per year, with 435 defined cancer procedures [26]
- Report/Committee: Standing Committee on Chemicals and Fertilisers, Report No. 33, August 2026 — no permanent trade margin framework, unrecovered overcharging dues, incomplete price data [15]
- Report/Committee: Parliamentary committee report on price rise of medicines — amend DPCO 2013 to allow trade margin rationalisation [16]
- Report/Committee: Standing Committee on Health and Family Welfare, 175th–177th Reports — PM-JAY's inpatient-only cover is inadequate [25]
- Report/Committee: WHO technical report on pricing of cancer medicines, 2018, under World Health Assembly Resolution 70.12 [21]
- Law/Case: Para 19, DPCO 2013 — power used for the cap [2]; non-scheduled drugs are limited to a 10% annual price rise [17]
- Comparison: WHO South-East Asia review — India is one of five countries in the region that set a ceiling on retail prices, and the review warns that several mark-up policies had harmful side effects [23]
- Comparison: WHO pricing guideline — use several policies together, including tendering and price transparency, to keep generic and biosimilar prices low [22]
- Scheme: AMRIT pharmacies — 289 cancer medicines through 217 outlets as of June 2025 [27]
- Scheme: PM-JAY — covers inpatient cancer care but leaves outpatient medicine costs to the patient [25][26]
15. Mains Relevance
- GS-II: Issues relating to development and management of social sector/services relating to Health; government policies and interventions.
- GS-III: Inclusive growth; effects of regulation on the pharmaceutical sector.
- Question stems: 1. "Trade margin rationalisation offers a targeted route to affordable medicines without direct price fixing." Critically examine with reference to anti-cancer drugs in India. 2. Discuss the adequacy of India's drug-price regulatory framework in reducing out-of-pocket expenditure on catastrophic illnesses. 3. Consumer-driven enforcement can supplement but not replace regulatory capacity. Examine in the context of medicine pricing in India.
16. Related Topics to Study Next
- DPCO 2013 and scheduled vs non-scheduled drugs: the legal core of this topic.
- National List of Essential Medicines: determines which drugs enter the First Schedule.
- Out-of-pocket health expenditure: the affordability problem the cap addresses.
- Trade margins on medical devices: the same policy question in an adjacent sector [14].
- AMRIT pharmacies: sell cancer drugs at substantial discounts to MRP [12].
- Customs duty exemptions on cancer medicines: a parallel, tax-side affordability lever [12].
- PLI for pharmaceuticals and medical devices: the supply-side counterpart to price control.
- Compulsory licensing and patents on cancer drugs: an alternative route to access for high-cost therapies.
17. NCERT Concepts to Revise
- Trade margin rationalisation (Economy): The core policy: capping the trader's margin at 30% of MRP on 137 anti-cancer drugs.
- Drugs (Prices Control) Order, 2013 (Economy): The legal framework, and its Para 19 public-interest power, that NPPA used for this cap.
- National Pharmaceutical Pricing Authority (Polity): The regulator that issued the cap, tracks revised MRPs and handles overcharging cases.
- Scheduled and non-scheduled drugs (Economy): This action covers non-scheduled drugs through a margin cap, unlike ceiling prices for scheduled drugs.
- National List of Essential Medicines (Economy): NLEM drugs form the First Schedule of DPCO, which separates scheduled from non-scheduled drugs.
- Maximum Retail Price (Economy): The cap works by lowering the MRP printed on packs, which consumers can check and complain about.
- Out-of-pocket expenditure (Economy): Cancer care causes heavy out-of-pocket spending and borrowing, which is the affordability problem the cap targets.
- Ayushman Bharat PM-JAY (Economy): It covers only inpatient care, so price cuts help with outpatient medicine bills it leaves out.
- Pharma Sahi Daam (Polity): NPPA's app, with the Pharma Jan Samadhan portal, lets consumers verify revised prices and report overcharging.
- Price control (Economy): The wider idea of government regulating prices, of which this margin cap is one form.
- Compulsory licensing (Economy): An alternative route to cheaper cancer drugs that works on patents, not on trade margins.
- Essential commodities (Economy): DPCO is issued under the Essential Commodities Act, which is the source of the government's price powers.
18. Common Errors / Trap Areas
- Wrong ministry: NPPA is not under the Health Ministry, even though DGHS constituted the committee [1].
- 137 vs 121 vs 1,364: 137 drugs were capped, 121 drugs had been reported by 8 November, and 1,364 is a count of formulations [1]. "1,364 drugs" is wrong.
- Scheduled vs non-scheduled: This is a Para 19 action on non-scheduled drugs, not a ceiling price for NLEM drugs [2][9].
- Projected vs reported: "Up to 70%" was the projection and 96.45% is the highest reported cut [1][2].
- Conflicting figures and dates:
- Savings: Use ₹3,540.38 crore, the latest figure tied to reported data [1], not ₹2,500 crore [7].
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Committee date: The digest gives 17 October 2026 as the date the committee was constituted [1]. That is also the Gazette date [2], so it may be a conflation. Check the release before memorising it.
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Standard facts not confirmed by a whitelisted source in this run, so verify them separately:
- NPPA's establishment in 1997.
- DPCO being issued under the Essential Commodities Act, 1955.
- The 10% annual MRP increase limit for non-scheduled drugs.
Sources
- 1Press Release Page (digest of the release on revised MRPs of 1,364 anti-cancer formulations)pib.gov.in · tier 1
- 2Trade Margin Rationalisation on 137 Anti-Cancer Drugspib.gov.in · tier 1
- 3NPPA has put a cap on Trade Margin of 42 select non-scheduled anti-cancer medicinespib.gov.in · tier 1
- 4Significant Reduction in Cancer Drug Prices due to Trade Margin Cappingpib.gov.in · tier 1
- 5MRP of 390 Anti-Cancer Non-Scheduled Medicines reduced up to 87%pib.gov.in · tier 1
- 6NPPA releases Revised MRP for 543 brands of Anti-Cancer Medicinespib.gov.in · tier 1
- 7Government Expands Cancer Medicine Price Controls; Cancer Patients Expected to Save ₹2,500 Crore Annuallypib.gov.in · tier 1
- 8Tata Memorial Centre and ACTREC Study on High Cost of Modern Cancer Drugspib.gov.in · tier 1
- 9NPPA fixes ceiling prices in respect of the drugs specified in Schedule-I to DPCO, 2013pib.gov.in · tier 1
- 10Prices of drugs in India are regulated as per the provisions of DPCO, 2013pib.gov.in · tier 1
- 11NPPA plays crucial role in making Cancer Drugs affordablepib.gov.in · tier 1
- 12Press Release: Press Information Bureau (cancer medicine affordability measures)pib.gov.in · tier 1
- 13Government of India, Chemicals and Fertilizers, Lok Sabha answereparlib.sansad.in · tier 1
- 14Issue of high trade margins in essential medical devicespib.gov.in · tier 1
- 15Monthly Policy Review, August 2026 (Standing Committee on Chemicals and Fertilisers report on NPPA)prsindia.org · tier 1
- 16Committee Reports: Price Rise of Medicines in the Pharmaceutical Sectorprsindia.org · tier 1
- 17Standing Committee on Chemicals and Fertilizers (2024-25), Eighth Reporteparlib.sansad.in · tier 1
- 18Overcharging by Drug Manufacturerpib.gov.in · tier 1
- 19Press Release Page (NPPA overcharging complaints, demand notices and recoveries)pib.gov.in · tier 1
- 20Exploitation of Consumers by Pharmaciespib.gov.in · tier 1
- 21Technical report: pricing of cancer medicines and its impactsapps.who.int · tier 2
- 22Country pharmaceutical pricing policiescdn.who.int · tier 2
- 23Medicines' price regulatory interventions in the WHO South-East Asia Region: policy review and recommendations for further researchcdn.who.int · tier 2
- 24PD-1/PD-L1 immune checkpoint inhibitors: financial impact report (2025 WHO Essential Medicines List Expert Committee)cdn.who.int · tier 2
- 25Press Release on the 175th, 176th and 177th Report of Parliamentary Standing Committee on Health & Family Welfarepib.gov.in · tier 1
- 26Explainer: World Cancer Day (February 04)static.pib.gov.in · tier 1
- 27Affordable and Accessible Healthcare for All, 17 June 2025static.pib.gov.in · tier 1