Nonclinical Safety Assessment
Autor: | William J. Brock, Kenneth L. Hastings, Kathy M. McGown |
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EAN: | 9781118516980 |
eBook Format: | ePUB |
Sprache: | Englisch |
Produktart: | eBook |
Veröffentlichungsdatum: | 05.03.2013 |
Untertitel: | A Guide to International Pharmaceutical Regulations |
Kategorie: | |
Schlagworte: | EMEA guidance ICH Kenneth Hastings Nonclinical Safety Assessment U.S. FDA WHO William Brock World Health Organization drug safety |
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It includes:
- ICH – the International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use
- National regulations, including US FDA, Canada, Mercosur and Brazil, South Africa, China, Japan, India and Australia
- Repeated dose toxicity studies
- Carcinogenicity; Genotoxicity; Developmental and reproductive toxicology; Immunotoxicology
- Biotechnology-derived pharmaceuticals
- Vaccine development
- Phototoxicity and photocarcinogenicity
- Degradants, impurities, excipients and metabolites
Primarily intended for those professionals actively involved in the nonclinical and clinical development of a pharmaceutical product, including toxicologists, pharmacologists, clinicians and project managers, this book provides a roadmap for successful new drug approval and marketing.
Dr. William J Brock, Brock Scientific Consulting, USA
Dr. Bill Brock is Principal of Brock Scientific Consulting and manages R&D programs for clients in the pharmaceutical, chemical, food and consumer product industries. He is the Past-President of American Board of Toxicology, serves on the Board of Directors for the Academy of Toxicological Sciences and is an Associate Editor for the International Journal of Toxicology. Dr. Brock has served in a leadership capacity in various organizations within the Society of Toxicology, the American College of Toxicology and is co-chair of the nonclinical section of the Drug Information Association.
Dr. Kenneth Hastings, sanofi-aventis, USA
Dr Hastings was Associate Director for Pharmacology/Toxicology in the Office of New Drugs, US Food and Drug Administration, from 2003 to 2007. He currently is Associate Vice President for Regulatory Policy at sanofi-aventis. He has served in several professional societies, including the American Board of Toxicology (currently President), the American College of Toxicology (currently President-Elect), the Society of Toxicology (Past President of the Immunotoxicology Specialty Section), and as Co-Chair of the Nonclinical Special Interest Committee of the Drug Information Association.