Regulatory affairs and pharmacological drug safety issues of Ayurvedic medicine has been overlooked by practitioners for many years. Research in Ayurveda is now a world-wide phenomenon, and several large pharmaceutical corporations are investing money for novel drug discovery from Ayurvedic sources. This book examines the regulatory and pharmacological aspects and includes extensive data on scientific evaluation carried out on Ayurvedic formulations. It will also serve as a reference book on standardization, pre-clinical studies, and clinical and toxicological studies on Ayurvedic formulations.

part A|96 pages

Ayurveda and Regulatory Affairs

chapter 1|5 pages

Introduction to Regulatory Affairs

chapter 4|4 pages

Ayurvedic Drug Manufacturing License

chapter 6|4 pages

Ayurvedic Drug Industry

chapter 7|5 pages

Pharmacovigilance of Ayurvedic Drugs

chapter 11|6 pages

Clinical Trials in Ayurveda

chapter 12|3 pages

National Ayush Mission

chapter 13|3 pages

Ayurvedic Pharmacy Education

chapter 15|2 pages

Ayurvedic Pharmacoepidemiology

chapter 17|2 pages

Ayurvedic Databases

part B|116 pages

Pharmacological Investigations on Ayurvedic Formulations

chapter |11 pages


chapter |3 pages


chapter |13 pages


chapter |11 pages


chapter |6 pages