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New Drug Development Chandrahas Sahajwalla (US Food and Drug Administration, Rockville, Maryland, USA)

New Drug Development By Chandrahas Sahajwalla (US Food and Drug Administration, Rockville, Maryland, USA)

Summary

Highlighting key points from the latest regulatory requirements, this book helps those new to the world of pharmaceutical development understand regulatory steps, reduce cost and attain guidance through each step of the drug approval process.

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New Drug Development Summary

New Drug Development: Regulatory Paradigms for Clinical Pharmacology and Biopharmaceutics by Chandrahas Sahajwalla (US Food and Drug Administration, Rockville, Maryland, USA)

Highlighting key points from the latest regulatory requirements, New Drug Development helps those new to the world of pharmaceutical development understand regulatory steps, reduce cost by avoiding unnecessary trials, and attain guidance through each step of the drug approval process. This volume acquaints readers with procedures that determine the success of drug development projects with updated regulatory guidelines from the FDA and ICH, solutions to hurdles in application protocols, and recommendations from more than 40 respected and experience officials from regulatory agencies around the globe. It covers topics related to the development of chiral drugs, liposomal products, and more.

New Drug Development Reviews

...the chapters are readable, the figures are clear in reproduction, the result being a useful text that I believe meets its goal of being an introductory text to drug development from a pharmacokinetic regulatory point-of-view.
-Pharmaceutical Research

...a timely book which combines the scientific and regulatory aspects of clinical pharmacology and biopharmaceutics in easy-to-understand chapters that cover all aspects of drug development....fills an existing void and further provides a quick reference guide for the industrial or academic scientist who is new in the field.-

. Janet Woodcock, M.D., Director, Center for Drug Evaluation and Research, and Acting Deputy Commissioner for Operations, Food and Drug Administration

Table of Contents

Introduction to Drug Development and Regulatory Decision-Making Larry Lesko; Evolution of Drug Development and its Regulatory Process Hank Malinowski; Regulatory Bases for Clinical Pharmacology and Biopharmaceutics Information in a New Drug Application Mehul Mehta; New Drug Application Content and Review Process for Clinical Pharmacology and Biopharmaceutics Chandra Sahajwalla; In-Vitro Drug Metabolism Studies During Development of New Drugs Shiew-Mei Huang; Drug Transporters Xiaoxiong Wei; Principles, Issues, and Applications of Interspecies Scaling Iftekhar Mahmood; Analytical Method Validation Brian Booth; Studies of the Basic Pharmacokinetic Properties of a Drug: A Regulatory Perspective Maria Sunzel; Surrogate Markers in Drug Development Jurgen Venitz; Population Pharmacokinetic and Pharmacodynamic Analysis Jogarao V. S. Gobburu; Scientific and Regulatory Considerations for Studies in Special Population Chandra Sahajwalla; Conducting Clinical Pharmacology Studies in Pregnant and Lactating Women Kathleen Uhl

Additional information

CIN0824754654G
9780824754655
0824754654
New Drug Development: Regulatory Paradigms for Clinical Pharmacology and Biopharmaceutics by Chandrahas Sahajwalla (US Food and Drug Administration, Rockville, Maryland, USA)
Used - Good
Hardback
Taylor & Francis Inc
20040524
500
N/A
Book picture is for illustrative purposes only, actual binding, cover or edition may vary.
This is a used book - there is no escaping the fact it has been read by someone else and it will show signs of wear and previous use. Overall we expect it to be in good condition, but if you are not entirely satisfied please get in touch with us

Customer Reviews - New Drug Development