Containing contributions from the many disciplines involved in a drug's evolution, this timely volume examines the entire pharmaceutical development process, emphasizing approaches to increasing efficiency and reducing costs.
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Inside This Book
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First Sentence:
Change is part of the human condition, but often we fail to notice the pace of change. Read the first page Key Phrases - Statistically Improbable Phrases (SIPs): (learn more)
clinical pathology support, drug development environment, supervisory investigator, clinical pathology testing, synthetic discovery, discovery portfolio, dissolution performance, mixed effect modeling, preferred supplier relationships, decentralized procedure, clinical development program, clinical pathology laboratory, drug interaction studies, drug development process, special patient populations, toxicokinetic studies, prospective planning, drug development program, foreign data, dissolution data, dissolution profile, study specifications, metabolism data, local laboratories, new drug development Key Phrases - Capitalized Phrases (CAPs): (learn more)
United States, New York, Marcel Dekker, European Union, Pharmaceutical Executive, Medicinal Chemistry, Applied Clinical Trials, Lyakuhin Kikou, Pharmaceutical Manufacturers Association, Reports-The Pink Sheet, Drug Information Journal, Standing Committee, Control Rel, Good Laboratory Practice, Orphan Drug Act, Physician's Desk Reference, Raven Press, Structural Biology, Annals of Oncology, Boca Raton, Council Directive, Council Regulation, Current Opinion, Good Manufacturing Practice, John Wiley New!
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Front Cover | Table of Contents | First Pages | Index | Back Cover | Surprise Me!
Change is part of the human condition, but often we fail to notice the pace of change. Read the first page Key Phrases - Statistically Improbable Phrases (SIPs): (learn more)
clinical pathology support, drug development environment, supervisory investigator, clinical pathology testing, synthetic discovery, discovery portfolio, dissolution performance, mixed effect modeling, preferred supplier relationships, decentralized procedure, clinical development program, clinical pathology laboratory, drug interaction studies, drug development process, special patient populations, toxicokinetic studies, prospective planning, drug development program, foreign data, dissolution data, dissolution profile, study specifications, metabolism data, local laboratories, new drug development Key Phrases - Capitalized Phrases (CAPs): (learn more)
United States, New York, Marcel Dekker, European Union, Pharmaceutical Executive, Medicinal Chemistry, Applied Clinical Trials, Lyakuhin Kikou, Pharmaceutical Manufacturers Association, Reports-The Pink Sheet, Drug Information Journal, Standing Committee, Control Rel, Good Laboratory Practice, Orphan Drug Act, Physician's Desk Reference, Raven Press, Structural Biology, Annals of Oncology, Boca Raton, Council Directive, Council Regulation, Current Opinion, Good Manufacturing Practice, John Wiley New!
Books on Related Topics | Concordance | Text Stats Browse Sample Pages:
Front Cover | Table of Contents | First Pages | Index | Back Cover | Surprise Me!
Citations (learn more)
This book cites 89
books:
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- Drug Toxicokinetics (Drug and Chemical Toxicology) by Welling on page 255, page 278, and page 279
- Good Manufacturing Practices for Pharmaceuticals: A Plan for Total Quality Control (Drugs and the Pharmaceutical Sciences Series, Vol 78) by Sidney H. Willig in Front Matter (1), Front Matter (2), and Front Matter (3)
- Pharmaceutical Statistics: Practical and Clinical Applications, Fourth Edition, Revised and Expanded (Drugs and the Pharmaceutical Sciences) by Sanford Bolton in Front Matter (1), Front Matter (2), and Front Matter (3)
- Modern Pharmaceutics by Gilbert S. Banker in Front Matter (1), Front Matter (2), and Front Matter (3)
- Drug Permeation Enhancement (Drugs and the Pharmaceutical Sciences) by Hsieh in Front Matter, and page 194
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