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實驗室調(diào)查(OOS)指導(dǎo)原則
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(1)fda-guidance for industry investigating out-of-specification (oos) test results for pharmaceutical production (2)mhra-out of specification investigations. 兩大權(quán)威指導(dǎo)原則,每次重讀都有新的收獲!更新MHRA指導(dǎo)原則[ Last edited by 1949stone on 2019-3-4 at 13:04 ] |
藥物申報與工藝設(shè)計 |


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