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....
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| Format: | eBook |
| Language: | English |
| Published: |
Chichester, West Sussex :
Wiley,
2013.
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| Subjects: | |
| Online Access: | Connect to the full text of this electronic book |
Table of Contents:
- Introduction to the development of drugs / Kathy McGown
- ICH / Ken Hastings
- USFDA / Bill Brock
- Latin America : MERCOSUR countries / Cristiana Leslie Corra
- Canada / Mark T. Goldberg
- EMEA / Adam Woolley
- Africa / Fariza Feraoun
- China / Lijie Fu
- Japan / Kazuichi Nakamura
- India / K.S. Rao
- Australia / Doug Francis
- Chronic repeat dose testing / Shana Azri-Meehan
- Carcinogenicity / James Popp
- Genotoxicity / Mark Powley
- Developmental and reproductive toxicology / Robert Parker
- Juvenile testing and pediatric claim / Melissa Tassinari
- Immunotoxicology / Leigh Ann Burns Naas
- Biologics / Chris Ellis
- Vaccines / Robert House
- Phototoxicity and photocarcinogenicity / Chris Sambuco
- Degradants, impurities excipients, and metabolites / Bob Osterberg.