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11#
發(fā)表于 2025-3-23 11:56:58 | 只看該作者
12#
發(fā)表于 2025-3-23 15:50:11 | 只看該作者
https://doi.org/10.1007/978-3-658-11928-7oratory to carry out actions that address risks and opportunities within the laboratory management program. These actions should be planned to improve the program so that testing can be performed properly, and most importantly can prevent failures in the laboratory. The ISO 17025:2017 prescribes tha
13#
發(fā)表于 2025-3-23 18:56:42 | 只看該作者
14#
發(fā)表于 2025-3-24 00:38:27 | 只看該作者
15#
發(fā)表于 2025-3-24 05:05:50 | 只看該作者
https://doi.org/10.1007/978-3-531-90237-1rol are the quality targets defined as the maximum possible error of imprecision and inaccuracy (absolute and relative error). Adherence to these targets during routine analysis must be monitored during the systematic repetition of control analyzes.
16#
發(fā)表于 2025-3-24 08:08:10 | 只看該作者
17#
發(fā)表于 2025-3-24 13:19:29 | 只看該作者
18#
發(fā)表于 2025-3-24 15:59:34 | 只看該作者
Control Charts and Process Capability,rol are the quality targets defined as the maximum possible error of imprecision and inaccuracy (absolute and relative error). Adherence to these targets during routine analysis must be monitored during the systematic repetition of control analyzes.
19#
發(fā)表于 2025-3-24 19:32:05 | 只看該作者
https://doi.org/10.1007/978-3-322-87289-0To verify any process and express the results in a form required by customer, a set of statistical procedures must be present along the chain of the analytical process.
20#
發(fā)表于 2025-3-25 00:06:20 | 只看該作者
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