Ghaziabad

The Indian Pharmacopoeia Commission (IPC) is an Autonomous Body under Ministry of Health & Family Welfare, Govt, of India primarily with the objectives of regularly updating the Indian Pharmacopoeia by publishing new edition and its addenda, National Formulary of India and other related tasks such as preparing, certification and distribution of reference substances & functions as National Coordination Centre (NCC) for Pharmacovigilance Programme of India (PvPI).

The Ministry of AYUSH was formed on 9th November 2014 to ensure the optimal development and propagation of AYUSH systems of health care. Earlier it was known as the Department of Indian System of Medicine and Homeopathy (ISM&H) which was created in March 1995 and renamed as Department of Ayurveda, Yoga and Naturopathy, Unani, Siddha and Homoeopathy (AYUSH) in November 2003, with focused attention for development of Education and Research in Ayurveda, Yoga and Naturopathy, Unani, Siddha and Homoeopathy.

Post : Research Officer

The Indian Pharmacopoeia Commission (IPC) is an Autonomous Body, set up under the Ministry of Health & Family Welfare, Government of India primarily with the objective of periodically updating of the Indian Pharmacopoeia (IP) that sets standards for the identity, safety, quality, and strength of medicines being manufactured and marketed in India.

Post : Pharmacopoeia Consultant

The Indian Pharmacopoeia Commission is an Autonomous Body set up under the Ministry of Health and Family Welfare, Govt. of India primarily with the objectives of regularly updating the Indian Pharmacopoeia by publishing new edition and its Addenda, National Formulary of India and other related tasks such as preparing, certification and distribution of Reference Substances.

Post : Pharmacopoeial Associate (Scientific)

The Indian Pharmacopoeia Commission, Sector-23, Raj Nagar, Ghaziabad-201002, an autonomous body set up under the Societies Registration Act, 1860 under the Ministry of Health & Family Welfare primarily with the objective of periodically bringing out new edition of India Pharmacopoeia, National Formulary of India and other related tasks such as preparing certification and distribution processes of other reference substances, is looking for a competent, dedicated and dynamic person for the post of Secretary-cum-Scientific Director as per details below.

Post : Secretary-cum - Scientific Director

The Indian Pharmacopoeia Commission (IPC) has been established as an autonomous Institution under the aegis of the Ministry of Health & Family Welfare, Govt. of India primarily with the objectives of regularly updating the Indian Pharmacopoeia (an official book for setting standards of drugs in the Country) by publishing new edition and its addenda, from time to time; National Formulary of India (reference book for rational use of generic medicines) and carrying out other related tasks such as providing Reference Substances to the stakeholders and conducting skill development programmes. The Commission also functions as National Coordination Centres (NCC) for Pharmacovigilance Programme of India (PvPI) and Materiovigilance Programme of India (MvPI) for ensuring safety of patients/drugs and medical devices, respectively, in the Country.

Raj Kumar Goel Institute of Technology ,Ghaziabad is one of the pioneer institute in the field of Pharmacy , Engineering and  Management.  RKGIT (PHARMACY) started its journey in the yea 2004 under the ablE guidance of Late Shri Raj Kumar Goel ji. The Institute offers B.Pharm and M.Pharm(Pharmaceutics)and is affiliated to Dr APJ AKTU, Lucknow and approved by AICTE and PCI.

The Indian Pharmacopoeia Commission (IPC) is an Autonomous Body,set up under the Ministry of Health &Family Welfare, Government of India primarily with the objective of periodically updating of the Indian Pharmacopoeia (IP) that sets standards for the identity, safety, quality, and strength of medicines being manufactured and marketed in India.

IPCis conducting walk-in interview for the engagement of Pharmacopoeia Consultantson contract basis with details as under.

Post : Pharmacopoeia Consultant

CENTRAL DRUGS STANDARD CONTROL ORGANIZATION, Under the Drug and Cosmetics Act, the regulation of manufacture, sale and distribution of Drugs is primarily the concern of the State authorities while the Central Authorities are responsible for approval of New Drugs, Clinical Trials in the country, laying down the standards for Drugs, control over the quality of imported Drugs, coordination of the activities of State Drug Control Organisations and providing expert advice with a view of bring about the uniformity in the enforcement of the Drugs and Cosmetics Act.