Quality Control of Homoeopathic Drugs

Homoeopathic   Pharmacopoeia   Committee   came into     existence   in 1962, as   the years   passed, methodology   and   parameters  got   concretized, quality   control   techniques  and   pharmaceutics became more   complicated   and   specialized. These necessitated    establishment    of     Drug Standardization   Units     and  later Homeopathic Pharmacopoeia   Laboratory.

Drug Standardization Units solely aimed towards standardization and quality control were established in 1972. it was also the period when Homoeopathic Pharmacopoeia Laboratory was established  in 1975 as a plan scheme. The scheme  envisaged a multi-disciplinary approach  towards

standardization and quality control of homoeopathic drugs. Speedy and pragmatic approach of the team in the implementation of the scheme helped in achievement of acceptable standards for commonly used homoeopathic medicines. Gradually there was establishment of a modern analytical laboratory, a herb garden, a herbarium and a museum of standard specimens relevant to homoeopathy in the country.

The laboratory grew as an apex institute for Pharmacopoeial standards and drug testing. It is an approved under Drugs and Cosmetics Act.

The laboratory grew as an apex institute for Pharmacopoeial standards and drug testing. It is an approved under Drugs and Cosmetics Act. The laboratory combines contemporary advanced technology with indigenous know-how and needs. Need based micro-modular approach has led to establishment of germ-plasm, seed  bank, a bank for back potency   for nosodes (homoeopathic bio-therapeutic agents), reference standard specimen bank for use in thin layer chromatography (TLC), gas liquid   chromatography    (GLC), high  pressure

liquid chromatography (HPLC), ultra-violet, infra-red and atomic absorption studies (UV, IR, AAS), pharmacological evaluation and screening. Laboratory has a computer based data information cell. Problems likely to be faced in the beginning of  the  next century have started surfacing gradually. To  face  them,  the   laboratory  envisages  quality monitoring,  drug evaluation cell,   programmes  for  plant  introduction  and  its

extension to hilly areas. Standardization towards perfection is an unending program. As the days pass the organization is getting better equipped to curb adulteration. Our efforts for achieving excellence in every field will continue.

As a result of continuous strenuous working of laboratory for laying down standards for identifying and testing of Homoeopathic medicines, Govt. of India, Ministry of Health & Family Welfare has published 8 volumes of Homoeopathic Pharmacopoeia of India containing 180 monograph in Vol. I, 100 in Vol. II, 105 in Vol. III, 107 in Vol. IV, 114 in Vol. V, 104 in Vol. VI, 105 in Vol. VII and 101 in Vol. VIII. All these monographs have duly been screened and approved by Homoeopathic Scientific Committee.

Website Developed, Designed & Maintained by PJSL