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Nonclinical Study Contracting and Monitoring
 
 

Nonclinical Study Contracting and Monitoring, 1st Edition

A Practical Guide

 
Nonclinical Study Contracting and Monitoring, 1st Edition,William Salminen,Joe Fowler,James Greenhaw,ISBN9780123978295
 
 
 

Salminen   &   Fowler   &   Greenhaw   

Academic Press

9780123978295

9780123978318

264

229 X 152

A hands-on guide complete with checklists, practical examples and sample reports to assist readers with the challenges of ensuring high-quality GLP studies.

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Key Features

  • Includes both the "big picture" look at complex processes, such as contracting toxicology and safety studies with CROs, as well as a detailed account of each individual step.
  • Contains several real world examples of problems in preclinical studies to provide you with an idea of the types of challenges that are routinely encountered and how this book can help you avoid these issues.
  • Provides monitoring checklists through the book that will help you comply with each GLP requirement and maintain compliance throughout the entire process.
  • Both entry level and experienced scientists involved in nonclinical toxicology study monitoring will benefit from the ideas, examples, discussions and strategies presented throughout this book.

Description

Nonclinical Study Contracting and Monitoring: A Practical Guide offers a systematic and straightforward handbook for obtaining high quality preclinical Good Laboratory Practice (GLP) studies. This book is full of real-world examples, processes, procedures, useful templates, checklists and sample reports to provide readers with a better understanding of exactly what happens during all stages of a GLP study and the critical aspects of GLP study design and conduct. Designed for both the novice and experienced scientist, this book covers the GLP regulations and how they impact preclinical studies, the differences between GLP, non-GLP and peer-reviewed studies, preclinical GLP study design, laboratory selection, contracts and business ethics, how to obtain test material for the study, animal sourcing and release for study, preparation of a draft report and much more. By illustrating the overall big picture and tying it together with the individual steps, this book is an essential resource to help scientists ensure a high quality GLP study that passes both scientific and regulatory scrutiny.

Readership

Toxicologists in pharmaceutical, agrochemical, food additive and industrial chemical industries, as well as study monitors, quality assurance unit (QUA) personnel, and other scientists who are responsible for contracting preclinical GLP studies with CROS and internal company laboratories.

William Salminen

Affiliations and Expertise

PhD, DABT, PMP, PAREXEL International, Benton, AR

Joe Fowler

Affiliations and Expertise

BS, RQAP-GLP, Director of the Quality Assurance Unit, National Center for Toxicological Research, FDA, Jefferson, AR

James Greenhaw

Affiliations and Expertise

BS, LAT, Director of the Quality Assurance Unit, National Center for Toxicological Research, FDA, Jefferson, AR

Nonclinical Study Contracting and Monitoring, 1st Edition

1. Introduction
2. Good Laboratory Practices
3. Study Design
4. Animal Welfare
5. Laboratory Selection
6. Project Proposal
7. Contracts and Business Ethics
8. Study Protocol, Preparation, Review, and Approval
9. Test Article
10. Study Start through End of In -Life
11. Study Communication and Data Management
12. A Study Director’s Perspective on Study Monitor-Study Director Interactions
13. Draft Report
14. Final Report, Study Close-Out, and Conclusions

Quotes and reviews

"I particularly liked the detailed checklists that are provided throughout the book…this book is an excellent practical guide on how to perform, contract, monitor and report nonclinical studies.  It is well presented and easy to read and will be particularly useful for beginning study monitors and toxicologists."--British Toxicology Society, Issue 43, Winter 2013

 
 

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