The Pharmacopoeia Commission for Indian Medicine and Homoeopathy and the Indian Pharmacopoeia Commission renewed their Memorandum of Understanding under the 'One Herb, One Standard' initiative for a further three years on 12 August 2026.
The MoU was exchanged at Kartavya Bhavan, New Delhi, in the presence of Prataprao Ganpatrao Jadhav, Minister of State (Independent Charge) for Ayush and Minister of State for Health and Family Welfare.
OHOS creates a single harmonised quality and testing standard, called a monograph, for a medicinal plant used across more than one system of medicine.
It covers plant-origin drugs used in five recognised systems: Ayurveda, Siddha, Sowa-Rigpa, Unani and Homoeopathy.
The first phase, begun in 2022, produced 50 single-herb monographs; the renewed phase will expand that set.
Develops pharmacopoeial standards for Ayurvedic, Siddha, Unani and Homoeopathic drugs, and functions as the Central Drug Testing cum Appellate Laboratory for these systems
Sets standards for drugs manufactured, sold and consumed in India, publishes the Indian Pharmacopoeia and the National Formulary of India, and runs the Pharmacovigilance Programme of India
The Pharmacopoeia Commission for Indian Medicine set up and registered as a society on 31 August 2010
Homoeopathy brought within its remit and the body renamed Pharmacopoeia Commission for Indian Medicine and Homoeopathy
Gazette notification reconstitutes PCIM&H as a subordinate office under the Ministry of Ayush, merging the Pharmacopoeial Laboratory for Indian Medicine and the Homoeopathic Pharmacopoeia Laboratory into it
First OHOS MoU signed in New Delhi between PCIM&H and IPC, launching phase 1
50 single-herb monographs jointly developed, with IPC carrying out phytochemical analysis
MoU renewed for three years at Kartavya Bhavan, New Delhi, opening the next phase of monograph development
Created in November 2014 by upgrading the Department of AYUSH; PCIM&H is one of its subordinate offices.
The official book of drug standards published by IPC; drugs conforming to it carry the I.P. suffix on their labels.
Run by IPC, it monitors adverse drug reactions and is the same commission's other headline function.
The parent legislation under which drug standards, including those for ASU and Homoeopathic drugs, are enforced.
The global centre for traditional medicine established in India, part of the same push to give Indian systems international standing.
The Ayush body promoting cultivation and conservation of medicinal plants, the supply side of the same quality chain.
GS Paper 2 > Government policies and interventions for development in various sectors; issues relating to health. GS Paper 3 > Indigenous technology and intellectual property in traditional knowledge
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A formal reference document fixing the identity, purity, strength and test methods for a drug substance.
An officially published book of drug standards that manufacturers and testing laboratories are required to follow.
Ayurveda, Siddha, Unani and Homoeopathy, the drug systems for which PCIM&H sets standards; OHOS extends the coverage to Sowa-Rigpa as well.
The traditional Himalayan system of medicine, recognised in India and practised chiefly in Ladakh, Himachal Pradesh, Sikkim and Arunachal Pradesh.
Laboratory identification and measurement of the chemical constituents of a plant, the technical work IPC contributes to monograph development.