你要知道ICH全称
International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use
ICH开始时的简称叫"三方协调会议", 就是美欧日这三方
说白了, 就是他们之间互相新药注册外加出口进口的, 每家的法规都不一样, 他们自己也烦死了, 就干脆坐在一起, 研究一些我们大家都认可的法规条目吧
发展到现在, 基本模式都是先在ICH上出指南, 之后各家再按着这个协调统一好的指南回去修改自己家的指南去, 你看看ICH Q9的影响力就能明白一二了
ICH是领跑的, 各家药监局跟着跑, CFDA是紧跟着EMA跑
ICH重要不重要自己看着办吧~~
ISPE与ICH是两回事吧
ISPE所有出版物上, 最前面都有一段话:
Disclaimer:
This Guide is meant to assist pharmaceutical manufacturers in the design and construction of new and renovated facilities that a
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发表于 2015-6-10 11:46
ISPE与ICH是两回事吧
ISPE所有出版物上, 最前面都有一段话:
Disclaimer:
This Guide is meant to assist pharmaceutical manufacturers in the design and construction of new and renovated facilities that are required to comply with the requirements of the US Food and Drug Administration (FDA). The International Society for Pharmaceutical Engineering (ISPE) cannot ensure, and does not warrant, that a facility built in accordance with this Guide will be acceptable to the FDA.
人家已经说得挺清楚啦
至于为什么大家不干脆直接按这个ICH, 查了一下ICH的mission http://www.ich.org/about/vision.html
ICH’s mission is to make recommendations towards achieving greater harmonisation in the interpretation and application of technical guidelines and requirements for pharmaceutical product registration, thereby reducing or obviating duplication of testing carried out during the research and development of new human medicines.
Harmonisation is achieved through the development of ICH Tripartite Guidelines. The Guidelines are developed through a process of scientific consensus with regulatory and industry experts working side-by-side. Key to the success of this process is the commitment of the ICH regulators to implement the final Guidelines.
ICH并不是大一统的法规机构, 其终旨也仅是为了协调与统一. 其产物是Guidelines. Guidelines终究只能是Guidelines, 把Guidelines变成法规, 就只能靠各家自己的监管部门啦~~