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Titlebook: Quality Control in Toxicology; G. E. Paget (Director) Book 1977 MTP Press Limited 1977 control.quality.quality control.research.toxicology

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书目名称Quality Control in Toxicology
编辑G. E. Paget (Director)
视频video
图书封面Titlebook: Quality Control in Toxicology;  G. E. Paget (Director) Book 1977 MTP Press Limited 1977 control.quality.quality control.research.toxicology
描述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.
出版日期Book 1977
关键词control; quality; quality control; research; toxicology; quality control, reliability, safety and risk
版次1
doihttps://doi.org/10.1007/978-94-011-7182-3
isbn_softcover978-94-011-7184-7
isbn_ebook978-94-011-7182-3
copyrightMTP Press Limited 1977
The information of publication is updating

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Some possible effects of the introduction of quality control systems on the discovery and safety evathe reading of the last editorial proof. With care, errors can be reduced to a minimum but rarely, if ever, excluded entirely. The regulatory function of a Government-appointed agency is to determine the predicted safety of a new drug on the evidence of pre-clinical toxicity work presented to them.
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The importance of experimental designl design. It is necessary, therefore, since every drug is unique, that the scientific and clinical evidence adequately demonstrates the safety and efficacy of the particular new product, and does not merely comply empirically with a series of toxicology check-lists. Moreover, data on the chemistry,
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Quality assurance in contract research organizationsary as ‘an attribute, property or special feature’. It was only about 100 years ago that the definition changed to include an element of ‘peculiar excellence or superiority’. Today, therefore, the most appropriate definition would seem to be:.The ..
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Some possible effects of the introduction of quality control systems on the discovery and safety evad Laboratory Practice: the only debate is the best means of achieving this, and we should keep constantly in our minds what should be the main purpose of our activities—which is, the introduction of significant new drugs of benefit to medicine, following an appraisal of the benefits and risks.
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Book 1977 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, o
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