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The Pharmacopoeia 2018 was released by Secretary, Ministry of Health & Family Welfare, Government of India. [ 5 ] I.P. , the abbreviation of 'Indian Pharmacopoeia' is familiar to the consumers in the Indian sub-continent as a mandatory drug name suffix.
Many developed countries set up their pharmacovigilance programs following the Thalidomide scandal in the 1960s. [2] India set up its program in the 1980s. [2] This general concept of drug safety monitoring went through different forms, but the Central Drugs Standard Control Organisation established the present Pharmacovigilance Program of India in 2010. [2]
The Indian government has announced its plan to bring all medical devices, including implants and contraceptives under a review of the Central Drugs and Standard Control Organisation (CDSCO). Within the CDSCO, the Drug Controller General of India (DCGI) regulates pharmaceutical and medical devices and is positioning within the Ministry of ...
Some further PV regulatory examples from the pharmerging nations are as follows. In India, the PV regulatory authority is the Indian Pharmacopoeia Commission, with a National Coordination Centre under the Pharmacovigilance Program of India, in the Ministry of Health and Family Welfare.
Download QR code; Print/export ... Indian Pharmacopoeia Commission; The International Pharmacopoeia; J. Japanese Pharmacopoeia; M.
Nitya Anand (1 January 1925 – 27 January 2024) was an Indian medicinal chemist who was the director of Central Drug Research Institute in Lucknow from 1974 to 1984. [1] [2] In 2005, Indian Pharmacopoeia Commission (IPC) appointed him chairman of its scientific committee. In 2012, he was awarded the Padma Shri by the Indian government. [3]
The 1699 Edinburgh Pharmacopoeia. 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.
Schedule H is a class of prescription drugs in India appearing as an appendix to the Drugs and Cosmetics Rules, 1945 introduced in 1945. These are drugs which cannot be purchased over the counter without the prescription of a qualified doctor.