FDA Regulatory Affairs: A Guide for Prescription Drugs, Medical Devices, and Biologics

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Douglas J. Pisano (St. Bonaventure University, New York, USA) David S. Mantus (Cubist Pharmaceuticals, Lexington, Massachusetts, USA)

FDA Regulatory Affairs

A Guide for Prescription Drugs, Medical Devices, and Biologics

Douglas J. Pisano (St. Bonaventure University, New York, USA), David S. Mantus (Cubist Pharmaceuticals, Lexington, Massachusetts, USA)

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English

CRC Press Inc
11 August 2008

Clinical trials; Pharmacology; Pharmacy & dispensing; Biology, life sciences; Pharmaceutical technology

Examines harmonization of the US Federal Food, Drug, and Cosmetic Act with international regulations as they apply to human drug and device development, research, manufacturing, and marketing. The Second Edition focuses on the new drug approval process, cGMPs, GCPs, quality system compliance, and corresponding documentation requirements. Written in a jargon-free style, it draws information from a wide range of resources. It demystifies the inner workings of the FDA and facilitates an understanding of how it operates with respect to compliance and product approval.

FDA Regulatory Affairs:

provides a blueprint to the FDA and drug, biologic, and medical device development offers current, real-time information in a simple and concise format contains a chapter highlighting the new drug application (NDA) process discusses FDA inspection processes and enforcement options includes contributions from experts at companies such as Millennium and Genzyme, leading CRO’s such as PAREXEL and the Biologics Consulting Group, and the FDA

Three all-new chapters cover:

clinical trial exemptions advisory committees provisions for fast track

Edited by: Douglas J. Pisano (St. Bonaventure University New York USA), David S. Mantus (Cubist Pharmaceuticals, Lexington, Massachusetts, USA)
Imprint: CRC Press Inc
Country of Publication: United States
Edition: 2nd edition
Dimensions: Height: 229mm, Width: 152mm, Spine: 28mm
Weight: 1.020kg
ISBN: 9781420073546
ISBN 10: 1420073540
Pages: 464
Publication Date: 11 August 2008
Audience: Professional and scholarly , Undergraduate
Format: Hardback
Publisher's Status: Active

DOUGLAS J. PISANO is Dean of the School of Pharmacy and Professor of Pharmacy Administration, Massachusetts College of Pharmacy and Health Sciences, Boston, Massachusetts, USA. Dr. Pisano received his Ph.D. in Law, Policy, and Society at Northeastern University, Boston, Massachusetts, USA. He is an active member of several professional organizations, including the American Association of Colleges of Pharmacy and the American Pharmaceutical Association. A national speaker and invited lecturer, Dr. Pisano was the recipient of the Special Service Award for the Enhancement of Regulatory Education from the Regulatory Affairs Professionals Society in 2000. He has developed several courses and programs at the Massachusetts College of Pharmacy and Health Sciences in such areas as health policy, pharmacy and drug law, and regulatory affairs. Dr. Pisano, along with coeditor Dr. David S. Mantus, is also the editor of the first edition of Informa Healthcare's FDA Regulatory Affairs: A Guide for Prescription Drugs, Medical Devices, and Biologics. DAVID S. MANTUS is Vice President of Regulatory Affairs and Program Management, Cubist Pharmaceuticals, Inc., Lexington; Adjunct Professor of Drug Regulatory Affairs, Massachusetts College of Pharmacy and Health Sciences, Boston; and President, C After D Inc., Boston, Massachusetts, USA. Dr. Mantus received his Ph.D. in Chemistry from Cornell University, Ithaca, New York, USA. He is an active member of the Regulatory Affairs Professional Society and the American Chemical Society and is a frequent presenter and lecturer at national conferences on biologics and biotechnology, regulatory affairs, and vaccine development. Dr. Mantus has also served as chairperson for several conferences, including ""Outsourcing Regulatory Affairs"" and ""Vaccine Development for the 21st Century.""