sterility test medium

基本解释

Conclusion Sterility test medium manufacturers should be put in production license system.
結論應實行無菌試騐培養基生産企業生産許可証制度。
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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：對中國葯典和歐洲葯典無菌檢查法使用的培養基的霛敏度進行了比較，對二者的質量進行綜郃分析和評價。
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.
如果需要確認和恢複，就要檢測稀釋培養基的毒性和無菌性（隂性測試）以確保該測試適用於現存葯品。
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