Preclinical Drug Development
. Ed(S): Rogge, Mark; Taft, David R.
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Description for Preclinical Drug Development
Preclinical Drug Development Editor(s): Rogge, Mark; Taft, David R. Series: Drugs and the Pharmaceutical Sciences. Num Pages: 376 pages, 58 black & white illustrations, 16 colour illustrations. BIC Classification: TDCW. Category: (P) Professional & Vocational. Dimension: 262 x 173 x 28. Weight in Grams: 884.
Preclinical Drug Development, Second Edition discusses the broad and complicated realm of preclinical drug development. Topics range from assessment of pharmacology and toxicology to industry trends and regulatory expectations to requirements that support clinical trials.
Highlights of the Second Edition include:
- Pharmacokinetics
- Modeling and simulation
- Formulation and routes of administration
- Toxicity evaluations
- The assessment of drug absorption and metabolism
- Interspecies scaling
- Lead molecule selection and optimization via profiling
- Screening using in silico and in vitro toxicity evaluations
The book also includes case studies on preclinical pharmacokinetic-pharmacodynamic modeling and simulation in drug development, a review of ICH preclinical guidelines, and experimental methods used to study ... Read more
Show LessProduct Details
Publication date
2009
Publisher
Taylor & Francis Inc United States
Number of pages
376
Condition
New
Series
Drugs and the Pharmaceutical Sciences
Number of Pages
380
Format
Hardback
Place of Publication
Bosa Roca, United States
ISBN
9781420084726
SKU
V9781420084726
Shipping Time
Usually ships in 4 to 8 working days
Ref
99-1
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