Published December, 2016
By Shayne Cox Gad and SC Gad
Publisher: John Wiley & Sons Ltd (Wiley-Blackwell)
Series: Pharmaceutical Development Series
Rating:
Availability: Available

This new edition of Drug Safety Evaluation offers a practical guide presents a road map for both the performance and evaluation of safety assessment as an integral part of the development of new drugs and therapeutics.

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Published January, 2012
By Shayne Cox Gad
Publisher: John Wiley & Sons Ltd (Wiley–Blackwell)
Series: Pharmaceutical Development Series
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Availability: Not available (reason unspecified)

This book is a one–stop compendium of up–to–date concepts, approaches, methodologies, and limitations in drug development and therapeutics. It provides researchers with a thorough reference focusing on applications, practical methods, and techniques to facilitate new drug development.

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Published July, 2009
By Shayne Cox Gad
Publisher: John Wiley & Sons Ltd (Wiley–Blackwell)
Series: Pharmaceutical Development Series
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Availability: Not available (reason unspecified)

This book provides a comprehensive and thorough reference on the basics and practices of clinical trials, arguably the most important steps in proving a drug effective and safe for public use. With contributions from a range of international authors, the book takes the reader through each trial phase, technique, and issue.

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Published July, 2009
By Shayne Cox Gad
Publisher: John Wiley & Sons Ltd (Wiley–Blackwell)
Series: Pharmaceutical Development Series
Rating:
Availability: Not available (reason unspecified)

Government regulatory agencies must approve any drug before it can be sold. This new edition of Drug Safety Evaluation presents a road map for safety assessment as an integral part of the development of new drugs and therapeutics.

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Published April, 2008
By Shayne Cox Gad and SC Gad
Publisher: John Wiley & Sons Ltd (John Wiley & Sons Inc)
Series: Pharmaceutical Development Series
Rating:
Availability: Available

This book gives the professional pharmaceutical scientist a basic and comprehensive tool to facilitate the preclinical development process by bringing together an overview of the preclinical process and a compendium of methods and techniques that need to be considered when developing a new drug.

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Published April, 2008
By Shayne Cox Gad
Publisher: John Wiley & Sons Ltd (Wiley–Blackwell)
Series: Pharmaceutical Development Series
Rating:
Availability: Not available (reason unspecified)

This book provides drug safety and toxicology scientists with practical guidance for testing and determining the effectiveness and safety of a new drug candidate. It authoritatively covers the important topics within toxicity testing, pharmacogenomics, and regulations for the preclinical safety testing of drug candidates.

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Published April, 2008
By Shayne Cox Gad
Publisher: John Wiley & Sons Ltd (Wiley–Blackwell)
Series: Pharmaceutical Development Series
Rating:
Availability: Not available (reason unspecified)

This book brings together in one resource an overview of the preclinical process along with a compendium of methods and techniques that need to be considered when developing a new drug.

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Published June, 2007
By Shayne Cox Gad
Publisher: John Wiley & Sons Ltd (Wiley–Blackwell)
Series: Pharmaceutical Development Series
Rating:
Availability: Not available (reason unspecified)

This Handbook describes the use of biotechnology to developpharmaceuticals. The process of biotechnological drug developmentsystematically identifies which protein is causing a problem in thebody ? either because it is absent, defective, or excessive ? andthen identifies and engineers a protein or related molecule tocorrect the problem.

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