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kk444555 在 2023-10-17 22:47 回答了问题
EMA
清洁验证完成之后,共用设施里的设备中更换产品时是否需要进行分析检测?
kk444555: Analytical testing is expected at each changeover unless justified otherwise via a robust, documented Quality Risk Management (QRM) process. The QRM p...
kk444555 在 2023-10-17 22:46 回答了问题
EMA
How can limits for cleaning purposes be established?
kk444555: Although the EMA guideline (EMA/CHMP/CVMP/SWP/169430/2012) may be used to justify cleaning limits (as per Introduction paragraph 3), it is not intende...
kk444555 在 2023-10-17 22:45 回答了问题
EMA
委托生产方在支持HBEL评估的数据方面有什么职责?
kk444555: Contract givers should either provide a full HBEL assessment to contract manufacturers or provide the data to allow the contract manufacturer to condu...
kk444555 在 2023-10-17 22:44 回答了问题
EMA
What competencies are required for the person developing the Health-Based Exposure Limits (HBEL)?
kk444555: Health-Based Exposure Limits should be determined by a person who has adequate expertise and experience in toxicology/pharmacology, familiarity with p...
kk444555 在 2023-10-17 22:43 回答了问题
EMA
How should manufacturers use the HBELs?
kk444555: The role of HBELs in determining cleaning limits is explained in Q&A 6. However, the purpose of generating HBELs goes beyond justification of clea...
kk444555 在 2023-10-17 22:42 回答了问题
EMA
有什么框架可以用来确定HBEL,用以广泛指导质量风险管理(QRM)的程度和是否需要控制措施?
kk444555: Firstly, it should be recognised that hazard varies on a continuum scale and that there are no firm cut off points, risk should be controlled on a pro...
kk444555 在 2023-10-17 22:41 回答了问题
EMA
Are Health-Based Exposure Limits (HBELs) required for all medicinal products?
kk444555: Yes, HBELs should be established for all medicinal products. The toxicological or pharmacological data, on which the HBEL calculation relies, requires...
kk444555 在 2023-10-17 22:40 回答了问题
EMA
生产过程中使用的设备变更,公司质量保证体系 (GMP) 涵盖哪些变更?
kk444555: Provided thatthe new equipment isequivalent to the one currently used, and operates in theapproved range ofprocess parameters, the change is covered b...
kk444555 在 2023-10-17 22:39 回答了问题
EMA
生产基地、厂房和房间的哪些变更可以由公司质量保证体系 (GMP) 覆盖?
kk444555: Provided thatmodule 3 is not impacted, withthe exception of section 3.2.A.1 (forbiological medicinalproducts), the changeslisted below (not an exhaust...
kk444555 在 2023-10-17 22:36 发表了文章
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