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The standards that are in effect since 1 December 2010, [4] are the Indian Pharmacopoeia 2010 (IP 2010). The Pharmacopoeia 2014 was released by Health Minister Ghulam Nabi Azad on 4 November 2013. [5] The Pharmacopoeia 2018 was released by Secretary, Ministry of Health & Family Welfare, Government of India. [5]
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]
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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 ...
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]
Indian National Congress (I) Rao: P. V. Narasimha Rao (12) B. Shankaranand (1925–2009) MP for Chikkodi: 18 January 1993 22 December 1994 1 year, 338 days – P. V. Narasimha Rao (1921–2004) MP for Nandyal (Prime Minister) 23 December 1994 11 June 1995 170 days: 21 A. R. Antulay (1929–2014) MP for Kolaba: 11 June 1995 16 May 1996 340 days ...
A travel expert revealed the science of why food and drinks taste different on a plane — and what he chooses to order once the beverage cart comes around.
In the 1980s, the European Union began harmonising regulatory requirements. In 1989, Europe, Japan, and the United States began creating plans for harmonisation. The International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use (ICH) was created in April 1990 at a meeting in Brussels.