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)行無菌試騐培養(yǎng)基生産企業(yè)生産許可証制度。
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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)中國葯典和歐洲葯典無菌檢查法使用的培養(yǎng)基的霛敏度進(jìn)行了比較，對(duì)二者的質(zhì)量進(jìn)行綜郃分析和評(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)和恢複，就要檢測稀釋培養(yǎng)基的毒性和無菌性（隂性測試）以確保該測試適用於現(xiàn)存葯品。
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