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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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樓主: BULB
11#
發(fā)表于 2025-3-23 09:46:14 | 只看該作者
12#
發(fā)表于 2025-3-23 15:54:58 | 只看該作者
A Swedish regulatory viewpointly and in different connexions, and we know that some toxicology investigations have been heavily criticized for not having been performed according to ‘good laboratory practice’. It thus seems well worth while to discuss the topic at some length. This is therefore the right conference at the right time, and may be at the right place.
13#
發(fā)表于 2025-3-23 22:04:06 | 只看該作者
Quality assurance in contract research organizationsary as ‘a(chǎn)n 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 ..
14#
發(fā)表于 2025-3-24 00:43:52 | 只看該作者
15#
發(fā)表于 2025-3-24 05:11:27 | 只看該作者
16#
發(fā)表于 2025-3-24 10:31:26 | 只看該作者
https://doi.org/10.1007/978-94-011-7182-3control; quality; quality control; research; toxicology; quality control, reliability, safety and risk
17#
發(fā)表于 2025-3-24 13:40:04 | 只看該作者
18#
發(fā)表于 2025-3-24 17:05:56 | 只看該作者
Quality control in an industrial laboratoryAs an introduction the following points must be made:
19#
發(fā)表于 2025-3-24 19:53:46 | 只看該作者
Good Laboratory Practices (GLPs) and the Bioresearch Monitoring ProgramIn order to provide some perspective for the basis and need for Good Laboratory Practices (GLP) regulations, I would first like to provide you with background information on Searle’s experience that led to the development of a Searle draft of Good Laboratory Practices in January, 1976 and FDA’s proposed regulations published on November 19, 1976.
20#
發(fā)表于 2025-3-24 23:33:33 | 只看該作者
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