E-Book, Englisch, 500 Seiten
Sahajwalla New Drug Development
1. Auflage 2004
ISBN: 978-0-203-02642-7
Verlag: Taylor & Francis
Format: PDF
Kopierschutz: Adobe DRM (»Systemvoraussetzungen)
Regulatory Paradigms for Clinical Pharmacology and Biopharmaceutics
E-Book, Englisch, 500 Seiten
Reihe: Drugs and the Pharmaceutical Sciences
ISBN: 978-0-203-02642-7
Verlag: Taylor & Francis
Format: PDF
Kopierschutz: Adobe DRM (»Systemvoraussetzungen)
Highlighting key points from the latest regulatory requirements, New Drug Development helps those new to the world of pharmaceutical development understand regulatory steps, reduce cost by avoiding unnecessary trials, and attain guidance through each step of the drug approval process. This volume acquaints readers with procedures that determine the success of drug development projects with updated regulatory guidelines from the FDA and ICH, solutions to hurdles in application protocols, and recommendations from more than 40 respected and experience officials from regulatory agencies around the globe. It covers topics related to the development of chiral drugs, liposomal products, and more.
Zielgruppe
) Pharmacists; pharmacologists; clinical investigators; pharmaceutical industry professionals involved in clinical, regulatory, statistical, and legal development of new drugs; and graduate and upper-level undergraduate students who intend to pursue careers in the pharmaceutical industry
