![]() ![]() Indian Pharmacopoeia contains procedures for analysis and specifications for the determination of quality of pharmaceutical substances, excipients and dosage forms. Publication of IP at regular and shorter intervals is one of the main mandates of the Commission. The Commission has been receiving significant inputs from regulatory, industrial houses, academic institutions, national laboratories, individual scientists and others. ![]() IP is published in continuing pursuit of the mission of IPC to improve the health of the people through ensuring the quality, safety and efficacy of medicines. It intends to help in the licensing of manufacturing, inspection and distribution of medicines. The standards of this pharmacopoeia are authoritative and legally enforceable. ![]() It prescribes the standards for drugs produced and/or marketed in India and thus contributes in the control and assurance of the quality of the medicines. The Indian Pharmacopoeia (IP) is published in fulfill of the requirements of the Drugs and Cosmetics Act, 1940 and Rules thereunder. The sixth edition of the Indian Pharmacopoeia (IP 2010) is published by the Indian Pharmacopoeia Commission (IPC) on behalf of the Government of India, Ministry of Health & Family Welfare. ![]()
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