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Pharmacokinetics in Drug Development

Regulatory and Development Paradigms (Volume 2)

Specificaties
Gebonden, blz. | Engels
American Assoc. of Pharm. Scientists | e druk, 2005
ISBN13: 9780971176737
Rubricering
American Assoc. of Pharm. Scientists e druk, 2005 9780971176737
€ 180,99
Levertijd ongeveer 8 werkdagen

Samenvatting

These volumes are designed to be the most complete guide to pharmacokinetics (PK) and its role in drug development. The volumes fill a gap between the academic science and the practical application of that knowledge in drug development. Volume 1 discusses the role that PK plays in selected clinical study designs. Volume 2 details the key regulatory and development paradigms in which PK supplements decision-making during drug development.

Specificaties

ISBN13:9780971176737
Taal:Engels
Bindwijze:gebonden
Uitgever:American Assoc. of Pharm. Scientists

Inhoudsopgave

Drug Development: A Rational Approach.- Experimental Design Considerations in Pharmacokinetic Studies.- Exposure-Response Relationships: A Critical Review of the FDA Guidance and Its Practical Utility.- Role fo Toxicology and Toxicokinetics in Drug Development.- Bioanaysis in a Regulated Environment.- Role of Preclinical Pharmacokinetics in Drug Development.- Pharmacokinetics/Pharmacodynamic Knowledge Discovery and Creation During Drug Development.- Regulatory Aspects of Clinical Pharmacokinetic Studies.- Regulatory Review of Pharmacokinetic Studies.- Regulatory Perspectives on Clinical Trial Simulations.- Nuances of Drug Metabolism and Pharmacokinetic Requirements for Package Submission to Japanese Regulatory Authorities.- Drug Development in Oncology.- Development of Chiral Compounds.- Development of Controlled-release Products.- Development Considerations for Biological Drugs.- Pharmacokinetics is Ocular Drug Development.- Development of Parenteral Dosage Forms.- Development of Transdermal Products.
€ 180,99
Levertijd ongeveer 8 werkdagen

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        Pharmacokinetics in Drug Development