風險管理是確保無菌藥品產(chǎn)品質量的關鍵因素之一。對無菌藥品生產(chǎn)、分析檢測等過程中的存在的風險因素進行識別和分析，進行風險等級的評估是進行無菌藥品質量風險管理的前提條件?？偨Y了無菌藥品生產(chǎn)過程的質量風險因素、無菌藥品生產(chǎn)質量風險評估和無菌藥品生產(chǎn)的質量風險控制，以期無菌藥品生產(chǎn)企業(yè)能夠顯著提升質量風險管理能力，進而創(chuàng)建一個高效、安全且穩(wěn)定的無菌藥品生產(chǎn)環(huán)境，確保最終產(chǎn)品的質量達到既定標準和規(guī)范。

Risk management is one of the key factors to ensure sterile drug product quality. Identifying and analyzing risk factors in the production, analysis, and testing process of sterile drugs, and conducting risk level assessments are prerequisites for quality risk management of sterile drugs. This article summarizes the quality risk factors in the production process of sterile drugs, the quality risk assessment of sterile drug production, and the quality risk control of sterile drug production, with the aim of significantly improving the quality risk management ability of sterile drug production enterprises, creating an efficient, safe, and stable sterile drug production environment, and ensuring that the final product quality meets established standards and specifications.

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