sterility test medium

基本解釋

Conclusion Sterility test medium manufacturers should be put in production license system.
結論應實行無菌試驗培養(yǎng)基生產企業(yè)生產許可證制度。
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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：對中國藥典和歐洲藥典無菌檢查法使用的培養(yǎng)基的靈敏度進行了比較，對二者的質量進行綜合分析和評價。
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.
如果需要確認和恢復，就要檢測稀釋培養(yǎng)基的毒性和無菌性（陰性測試）以確保該測試適用于現(xiàn)存藥品。
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