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हिन्दी — Read in HindiDrugs, diagnostics and medical technology
Drug approval and trials, the pharmacopoeia, substandard medicines, generics, prices, devices and pharmacovigilance. It serves GS3 answers on science and technology in health.
Foundation note: Who regulates medicines in India, and the drug schedules
Showing 2 of 10 articles, those that changed from 1 to 30 September 2026.Show all
Indian Pharmacopoeia Commission
Copy link to Indian Pharmacopoeia CommissionPrelims
A pharmacopoeia is the official book of standards a medicine must meet for identity, purity and strength, and India's is written by the Indian Pharmacopoeia Commission (IPC).
- Setting those standards is one half of the Commission's work; the other is watching what medicines and devices do once they are in use.
Works under
- Ministry of Health and Family Welfare
Publishes
- The Indian Pharmacopoeia, the official drug standards under the Drugs and Cosmetics Act, 1940
Runs
- Pharmacovigilance Programme of India
- Materiovigilance Programme of India
What changed
21 Sep 2026
- A Biovigilance Programme of India, led by the Commission, will track adverse events from products used in organ and tissue transplantation.
- It is the third safety track, after pharmacovigilance for medicines and materiovigilance for medical devices.
4 Aug 2026BriefThe WHO South East Asia Regulatory Network (SEARN) named the IPC its Regional Centre of Excellence in Pharmacovigilance. The IPC is also the network's Technical Centre in Quality of Medicines. PIB, 4 Aug 2026: Indian Pharmacopoeia Commission named WHO-SEARN Centre of Excellence (opens in a new tab)
24 Jun 2026BriefAmendment List 09 to IP 2022, in force from 10 October 2025, mandates the test for ethylene glycol and diethylene glycol in all oral liquid formulations. IP 2026 is the first pharmacopoeia with dedicated monographs for blood and blood components. PIB, 24 Jun 2026: IPC Successfully Conducts 2nd Hands-on Training on Ethylene Glycol (EG) and Diethylene Glycol (DEG) Determination in Oral Liquid Preparations by Gas Chromatography (opens in a new tab) · PIB, 24 Jun 2026: IPC Organizes National Conference on Ensuring Quality of Blood and Blood Components through IP 2026 Standards (opens in a new tab)
Rare diseases and orphan drugs
Copy link to Rare diseases and orphan drugsPrelims and Mains
An orphan drug is a medicine for a rare disease, long neglected by drug makers because the market for it is small.
- Government support for a patient with a rare disease is capped at ₹50 lakh, and there is a government crowdfunding platform for patients.
- The drug regulator may waive a local clinical trial for a drug already approved in certain other countries.
What changed
29 Sep 2026New
- India has reported about 1,000 rare genetic disorders, and drugs exist for only about 5 per cent of rare diseases.
Mains: incentives for manufacture, advance purchase commitments and pricing that shares benefits could make India a base for affordable orphan drugs.