sterility test medium

基本解釋

Conclusion Sterility test medium manufacturers should be put in production license system.
結(jié)論應(yīng)實(shí)行無(wú)菌試驗(yàn)培養(yǎng)基生產(chǎn)企業(yè)生產(chǎn)許可證制度。
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Objective:Comparing the sensitivity of test for sterility medium in ChP with that in EP, analyzing and evaluating their qualities.
目的：對(duì)中國(guó)藥典和歐洲藥典無(wú)菌檢查法使用的培養(yǎng)基的靈敏度進(jìn)行了比較，對(duì)二者的質(zhì)量進(jìn)行綜合分析和評(píng)價(jià)。
In the case of validation, recovery, toxicity of the dilution medium and sterility (negative test) are examined to guarantee the suitability of the test in the presence of the product.
如果需要確認(rèn)和恢復(fù)，就要檢測(cè)稀釋培養(yǎng)基的毒性和無(wú)菌性（陰性測(cè)試）以確保該測(cè)試適用于現(xiàn)存藥品。
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