A clear, straightforward resource to guide you through preclinical drug development Following this book's step-by-step guidance, you can successfully initiate and complete critical phases of preclinical drug development. The book serves as a basic,comprehensive reference to prioritizing and optimiz
Preclinical Development of Low Toxicity Drugs
โ Scribed by Dr Gillian D. Dines, Richard Bethell, Mick Daniel
- Book ID
- 119925032
- Publisher
- Springer International Publishing AG
- Year
- 1998
- Tongue
- English
- Weight
- 139 KB
- Volume
- 19
- Category
- Article
- ISSN
- 0114-5916
No coin nor oath required. For personal study only.
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*A Comprehensive Guide to Toxicology in Preclinical Drug Development* is a resource for toxicologists in industry and regulatory settings, as well as directors working in contract resource organizations, who need a thorough understanding of the drug development process. Incorporating real-life case
A clear, straightforward resource to guide you through preclinical drug development Following this book's step-by-step guidance, you can successfully initiate and complete critical phases of preclinical drug development. The book serves as a basic,comprehensive reference to prioritizing and optimiz