Nonclinical Safety Assessment : a Guide to International Pharmaceutical Regulations.

Bringing a new drug to market is a costly time-consuming process. Increased regional and international regulation over the last twenty years, while necessary, has only served to amplify these costs. In response to this escalation, developmental strategies have shifted towards a more global approach....

Full description

Bibliographic Details
Call Number:Libro Electrónico
Main Author: Brock, William
Other Authors: Hastings, Kenneth, McGown, Kathy M.
Format: Electronic eBook
Language:Inglés
Published: Hoboken : Wiley, 2013.
Subjects:
Drug development > International cooperation.
Drugs > Toxicology > International cooperation.
International cooperation.
Drug Evaluation, Preclinical > standards
Drug Approval > methods
Drug-Related Side Effects and Adverse Reactions > prevention & control
International Cooperation
Legislation, Drug
Toxicity Tests > standards
Médicaments > Développement > Coopération internationale.
Médicaments > Toxicologie > Coopération internationale.
Coopération internationale.
MEDICAL > Pharmacology.
International cooperation
Online Access:Texto completo

Internet

Texto completo

Items no disponibles

Holdings details from

Similar Items