Standardisation of Homoeopathic Drugs - Volume 1
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Standardisation of Homoeopathic Drugs - Volume 1

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Item Code: NAW912
Author: Chaturbhja Nayak
Publisher: Central Council for Research in Homoeopathy, New Delhi
Language: English
Edition: 2005
ISBN: 9788100000116
Pages: 140 (Throughout Color Illustrations)
Cover: PAPERBACK
Other Details: 11.00 X 8.50 inch
Weight 400 gm
Preface
Homoeopathic Materia Medica contains a large number of drugs of Plant, Chemical and Animal origin, whose standardization is essential 'to ensure safety, efficacy and quality. It involves identification of exact source materials. and other parameters which define pharmaceutical uniformity. Standards of Homoeopathic drugs are drawn on the basis of studies on pharmacognostical, physic-chemical and pharmacological parameters for each drug. The Pharmacognostical studies include macro and macroscopically characteristics of raw drugs of vegetable origin.

The survival, existence and the potential of a system of medicine solely depends upon the purity, quality, genuineness and the authenticity the drugs used by the system. Hence, Drug Standardization plays a prime role in the development of the particular system of medicine; The Homoeopathic System of Medicine mainly uses drugs of plant origin. The Central Council for Research in Homoeopathy has conducted Drug Standardization studies of more than 200 plants used in the system of Homoeopathic treatment.

The present work has been carried out at the four Drug Standardization Centers of the Council viz., Central Research Institute (Homoeopathy), Kolkata, Homoeopathic Drug Research Institute, Luck now, Drug Stand- radiation Units at Ghaziabad and Hyderabad, embodying detailed studies of the drugs from pharmacognostical, physicochemical and pharmacological aspects.

I hope that this contribution will be of great interest and use to the medical profession, pharmacognosists, academicians, researchers, pharmaceutical industries and Homoeopathic professionals in particular.

I gratefully acknowledge the guidance and advice received for the above study from the members of the Scientific Advisory Committee and Sub-committee on Drug Standardization of the Council.

My sincere thanks are due to the Scientists involved with the work for their contribution for the study and compilation of the work.

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