Quality Control in Toxicology

Author:   G.E. Paget
Publisher:   Springer
Edition:   Softcover reprint of the original 1st ed. 1977
ISBN:  

9789401171847


Pages:   128
Publication Date:   07 March 2012
Format:   Paperback
Availability:   Manufactured on demand   Availability explained
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Quality Control in Toxicology


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Overview

Topics in Toxicology Toxicology is a science that stands at the intersection of several interests and disciplines. These intersecting forces are by no means all scientific since some are legal and some are commercial. All have valid things to say about the conduct and interpretation of toxicity experiments. The practising toxicologist must bear all these sometimes conflicting forces in mind as he carries out his duties. This is especially true, of course, of the toxicologist in industry. Toxicology is also a field in which contract research particularly flourishes and a number of major contract research companies have established over the years a reputation for contributing usefully to the practice of this skill. These contract research organisations are particu­ larly favoured to develop an appreciation of the problems of the in­ dustrial toxicologist, since it is very common for such a company to service the toxicological needs of companies in several sectors of industry producing new chemical compounds, and the contract research company, therefore, is aware of a wider diversiy of problems than probably affects a single toxicologist in one industry.

Full Product Details

Author:   G.E. Paget
Publisher:   Springer
Imprint:   Springer
Edition:   Softcover reprint of the original 1st ed. 1977
Dimensions:   Width: 15.20cm , Height: 0.80cm , Length: 22.90cm
Weight:   0.226kg
ISBN:  

9789401171847


ISBN 10:   940117184
Pages:   128
Publication Date:   07 March 2012
Audience:   Professional and scholarly ,  Professional & Vocational
Format:   Paperback
Publisher's Status:   Active
Availability:   Manufactured on demand   Availability explained
We will order this item for you from a manufactured on demand supplier.

Table of Contents

Section One The Regulatory Viewpoint.- 1 Maintaining the creative balance.- 2 A Swedish regulatory viewpoint.- 3 The seven deadly sins—a U.K. view.- Section Two The Industrial Viewpoint.- 4 Some possible effects of the introduction of quality control systems on the discovery and safety evaluation of drugs.- 5 Quality control in an industrial laboratory.- 6 Good Laboratory Practices (GLPs) and the Bioresearch Monitoring Program.- Section Three The Independent Expert.- 7 Quality and integrity assurance.- 8 The importance of experimental design.- Section Four The Research Contractor.- 9 Quality assurance in contract research organizations.- 10 Some problems in good laboratory practice for a contract research laboratory.

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