A TEXTBOOK OF DRUG REGULATORY AFFAIRS

This book has been written to create a road map for the aspects of Drugs, Biologics, Medical devices as well as Nutraceuticals in U.S.A, Europe, India. This book covers the legal regulations and requirements of the above-mentioned aspects and the laws about their development. It is meant to be a concise reference that offers current, real-time information. The book can be used as a handy reference by students, staff and professionals at corporations, organizations and colleges belonging to this particular field. The new courses lay great emphasis on legislations & regulations of various countries in particular and other professional aspects in general.

Autorentext

Dr.P.Shailaja, working as an Associate professor in Andhra University, having more than 15 years of teaching experience. Dealing with research projects for PhD, M. Pharm/B. Pharm and Pharm D since 7 years. Has published many review articles in Pharmaceutical Drug Regulatory Affairs.