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Cost-Contained Regulatory Compliance: For the Pharmaceutical, Biologics, and Medical Device Industries
Sandy Weinberg
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Description for Cost-Contained Regulatory Compliance: For the Pharmaceutical, Biologics, and Medical Device Industries
Hardcover. This book guides the reader through FDA regulation guidelines and outlines a comprehensive strategy for cost reduction in regulatory affairs and compliance. This book explains six strategies to cost-effectively comply with FDA regulations while maintaining product safety and improving public access through cost controls. Num Pages: 296 pages, Illustrations. BIC Classification: KNDP; MMG; TDCW. Category: (P) Professional & Vocational. Dimension: 236 x 163 x 21. Weight in Grams: 560.
This book guides the reader through FDA regulation guidelines and outlines a comprehensive strategy for cost reduction in regulatory affairs and compliance. This book explains six strategies to cost-effectively comply with FDA regulations while maintaining product safety and improving public access through cost controls. It provides useful and practical guidance through industry case studies from pharmaceutical, biotech, and medical device industries.
This book guides the reader through FDA regulation guidelines and outlines a comprehensive strategy for cost reduction in regulatory affairs and compliance. This book explains six strategies to cost-effectively comply with FDA regulations while maintaining product safety and improving public access through cost controls. It provides useful and practical guidance through industry case studies from pharmaceutical, biotech, and medical device industries.
Product Details
Format
Hardback
Publication date
2011
Publisher
John Wiley & Sons Inc United Kingdom
Number of pages
296
Condition
New
Number of Pages
296
Place of Publication
New York, United States
ISBN
9780470552353
SKU
V9780470552353
Shipping Time
Usually ships in 7 to 11 working days
Ref
99-50
About Sandy Weinberg
SANDY WEINBERG, PhD, is a professor of healthcare management at Clayton State University in Atlanta and an international regulatory consultant. He has thirty-five years' regulatory experience, including global executive responsibility at GE Healthcare and Tikvah Therapeutics. Dr. Weinberg has written thirteen books including, most recently, Guidebook for Drug Regulatory Submissions, also from Wiley.
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