Generic Drug Product Development
Solid Oral Dosage Forms
Published on 31. October 2014
408 pages
978-1-4200-3041-9 (ISBN)
Description
Keeping pace with the latest technologies in the field, this guide describes the development of solid oral generic drug products from project initiation to market approval. Focusing on immediate-release and modified-release dosage forms, the book collects in-depth discussions from more than 30 noted specialists on topics such as quality control, ex
Reviews / Votes
"...interesting and varied reading....well written and edited. There is a good blend of authors from academia, the pharmaceutical industry, and the FDA...."...useful for those working, or having an interest in generic pharmaceutical manufacture and regulation."
-International Journal of Pharmaceutics
More details
Series
Language
English
Place of publication
Baton Rouge
United States
Publishing group
Taylor & Francis Inc
Target group
Professional and scholarly
Pharmacists; pharmacologists; clinical investigators; pharmaceutical industry professionals involved in clinical, regulatory, statistical, and legal development of generic drugs; and graduate and upper-level undergraduate students who intend to pursue careers in the pharmaceutical industry
Illustrations
5 s/w Photographien bzw. Rasterbilder
5 halftones
File size
3,58 MB
ISBN-13
978-1-4200-3041-9 (9781420030419)
Copyright in bibliographic data and cover images is held by Nielsen Book Services Limited or by the publishers or by their respective licensors: all rights reserved.
Schweitzer Classification
Other editions
Additional editions
Book
12/2004
1st Edition
Marcel Dekker Inc
€143.61
Article exhausted; check for reprint
