Items related to New Drug Approval Process (Drugs and the Pharmaceutical...
Synopsis
Reflects current rules, regulations, and guidelines in Title 21 of the Code of Federal Regulations and presents the latest advances in expediting drug development procedures. The book is designed to be of interest to research and development personnel in the pharmaceutical industry, including clinical and research pharmacists and pharmacologists, organic, medicinal, cosmetic, analytical, and clinical chemists and biochemists, clinical toxicologists, biostatisticians, government regulatory personnel, international pharmaceutical manufacturers and students in drug development courses.
"synopsis" may belong to another edition of this title.
Review
..."a useful road map to understanding the requirements that a drug product must fulfill to achieve approval." Journal of Medicinal Chemistry "There are very useful formats, brochures, statistics, addresses and checklists provided...in order to have a clean picture of the entire drug approval process. "The book has accomplished the laborious task of obtaining about 600 indispensable acronyms.a must for researchers, libraries, project consultants and...regulatory personnel." Pharmaceutical Development and Technology
"About this title" may belong to another edition of this title.
- PublisherMarcel Dekker Inc
- Publication date1987
- ISBN 10 0824773829
- ISBN 13 9780824773823
- BindingHardcover
- LanguageEnglish
- Number of pages469
Search results for New Drug Approval Process (Drugs and the Pharmaceutical...
Stock Image
New Drug Approval Process : Clinical and Regulatory Management (Drugs and the Pharmaceutical Sciences Ser., No. 30)
Published by
Marcel Dekker Incorporated, New York, NY, U.S.A., 1987
ISBN 10: 0824773829
ISBN 13: 9780824773823
Used
Hardcover
First Edition
Signed
Seller: Top Notch Books, Tolar, TX, U.S.A.
Seller rating 5 out of 5 stars
Hard Cover. Condition: Fine. No Jacket. First Printing. Delineates the most expeditious methods for bringing new prescription and over-the-counter drugs into the marketplace. Burgundy boards have almost no signs of wear. Guarino's inscription dated 10/16/87, on fep. Pages are bright, text clean & unmarked, binding is tight. Size: 8vo - over 7¾" - 9¾" tall. Inscribed by Author. Seller Inventory # 350017A
Quantity: 1 available
Stock Image
New drug approval process: Clinical and regulatory management (Drugs and the pharmaceutical sciences)
Seller: HPB-Red, Dallas, TX, U.S.A.
Seller rating 5 out of 5 stars
hardcover. Condition: Good. Connecting readers with great books since 1972! Used textbooks may not include companion materials such as access codes, etc. May have some wear or writing/highlighting. We ship orders daily and Customer Service is our top priority! Seller Inventory # S_426449618
Quantity: 1 available