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
Rezensionen / Stimmen
"...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
Reihe
Sprache
Verlagsort
Verlagsgruppe
Zielgruppe
Für Beruf und Forschung
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
Illustrationen
5 s/w Photographien bzw. Rasterbilder
5 halftones
Dateigröße
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 Klassifikation
