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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]
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 ...
Download QR code; Print/export ... Indian Pharmacopoeia Commission; The International Pharmacopoeia; J. Japanese Pharmacopoeia; M.
Download QR code; Print/export Download as PDF; ... Indian Pharmacopoeia Commission; M. Maharashtra State Pharmacy Council; N. National Pharmaceutical Pricing ...
Bishnupada Mukerjee (1 March 1903 – 30 July 1979) [1] or Bishnupada Mukhopadhyaya was an Indian pharmacologist [2] [3] and orthopedic surgeon, [4] known for his contributions in the fields of pharmacological research and standardization of drugs in India.
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.
Formulation studies involve developing a preparation of the drug which is both stable and acceptable to the patients. For orally administered drugs, this usually involves incorporating the drug into a tablet or a capsule.