search for books and compare prices
The Generic Challenge: Understanding Patents, FDA and Pharmaceutical Life-Cycle Management
Price
Store
Arrives
Preparing
Shipping
Jump quickly to results on these stores:
The price is the lowest for any condition, which may be new or used; other conditions may also be available.
Jump down to see edition details for: Paperback
Bibliographic Detail
Publisher
Brown Walker Pr
Publication date
November 30, 2013
Pages
194
Binding
Paperback
Edition
4th
Book category
Adult Non-Fiction
ISBN-13
9781612337289
ISBN-10
1612337287
Dimensions
0.50 by 5.50 by 8.25 in.
Weight
0.60 lbs.
Original list price
$35.95
Amazon.com says people who bought this book also bought:
Understanding Pharma: The Professional's Guide to How Pharmaceutical and Biotech Companies Really Work | The BioTech Primer | Valuation in Life Sciences | Pharmaceutical Lifecycle Management | Anda Litigation | Genentech | Generic | The Antidote | New Drugs
Understanding Pharma: The Professional's Guide to How Pharmaceutical and Biotech Companies Really Work | The BioTech Primer | Valuation in Life Sciences | Pharmaceutical Lifecycle Management | Anda Litigation | Genentech | Generic | The Antidote | New Drugs
Summaries and Reviews
Editions
Paperback
The price comparison is for this edition
4th edition from Brown Walker Pr (November 30, 2013)
9781612337289 | details & prices | 194 pages | 5.50 × 8.25 × 0.50 in. | 0.60 lbs | List price $35.95
3 edition from Brown Walker Pr (March 31, 2011); titled "The Generic Challenge: Understanding Patents, FDA & Pharmaceutical Life-Cycle Management"
9781599425764 | details & prices | 174 pages | 5.50 × 8.25 × 0.75 in. | 0.50 lbs | List price $28.95
2 edition from Brown Walker Pr (May 30, 2008); titled "The Generic Challenge: Understanding Patents, FDA & Pharmaceutical Life-Cycle Management"
9781599424446 | details & prices | 183 pages | 5.50 × 8.50 × 0.50 in. | 0.55 lbs | List price $28.95
About: Explains clearly and understandably the role of patents, FDA regulations of generic drugs and the Hatch Waxman Act on conventional and biological drug product development today and how directed innovation can result in enhanced care for patients while extending the commercial lives of the drugs.
About: Explains clearly and understandably the role of patents, FDA regulations of generic drugs and the Hatch Waxman Act on conventional and biological drug product development today and how directed innovation can result in enhanced care for patients while extending the commercial lives of the drugs.
from Brown Walker Pr (January 31, 2005)
9781581124309 | details & prices | 116 pages | 5.75 × 8.75 × 0.25 in. | 0.25 lbs | List price $24.95
About: The Generic Challenge is a must read for pharmaceutical executives and managers, and regulatory, legal, business development, R&D and strategic marketing professionals and anyone who has an interest in the future of the leading American pharmaceutical and biotechnology industries and the high value jobs they provide.
About: The Generic Challenge is a must read for pharmaceutical executives and managers, and regulatory, legal, business development, R&D and strategic marketing professionals and anyone who has an interest in the future of the leading American pharmaceutical and biotechnology industries and the high value jobs they provide.
Pricing is shown for items sent to or within the U.S., excluding shipping and tax. Please consult the store to determine exact fees. No warranties are made express or implied about the accuracy, timeliness, merit, or value of the information provided. Information subject to change without notice. isbn.nu is not a bookseller, just an information source.