![]() During quality assurance and at the time of dispute in the court of law the IP standards are legally acceptable. The standards of the IP are authoritative in nature and are enforced by the regulatory authorities for ensuring the quality of drugs in India. ![]() ![]() IP contains a collection of authoritative procedures of analysis and specifications of drugs for their identity, purity and strength. IP is recognized as the official book of standards for the drugs being manufactured and/or marketed in India. Indian Pharmacopoeia (IP) is published by the Indian Pharmacopoeia Commission (IPC) on behalf of the Ministry of Health & Family Welfare, Government of India in fulfilment of the requirements of the Drugs and Cosmetics Act, 1940 and Rules 1945 thereunder. IP 1996.Įdition Year Volumes Addendum/Supplement of Indian Pharmacopoeia The titles are suffixed with the respective years of publication, e.g. list was first published in the year 1946 and was put forth for approval. The actual process of publishing the first Pharmacopoeia started in the year 1944 under the chairmanship of Col. ![]() A pharmacopoeia, pharmacopeia, or pharmacopoea (from the obsolete typography pharmacopœia, meaning “drug-making”), in its modern technical sense, is a book containing directions for the identification of compound medicines and published by the authority of a government or a medical or pharmaceutical society History of Indian Pharmacopoeia IP ![]()
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