征求意见稿draft.pdf
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1、征求意见稿 draft【篇一:who 数据与记录管理规范指南 征求意见稿】guidance on good data and record management practices draft for comment en 2015/09 pdf 原文地址 working document qas/15.624 should you have any comments on the attached text,please send these to dr s.kopp,group lead,medicines quality assurance,technologies,standards
2、and norms(koppswho.int)with a copy to ms marie gaspard(gaspardmwho.int)by 30 november 2015.medicines quality assurance working documents will be sent out electronically only and will also be placed on the medicines website for comment under“current projects”.if you do not already receive our draft w
3、orking documents please let us have your email address(to bonnywwho.int)and we will add it to our electronic mailing list.schedule for the proposed adoption process of document qas/15.624:guidance on good data and record management practices background during an informal consultation on inspection,g
4、ood manufacturing practices and risk management guidance in medicines manufacturing held by the world health organization(who)in geneva in april 2014 a proposal for new guidance on good data management was discussed and recommended to be developed.the participants included national inspectors and sp
5、ecialists in the various agenda topics,as well as staff of the prequalification team(pqt)inspections.the who expert committee on specifications for pharmaceuticals preparations received feedback from this informal consultation during its 49th meeting held in october 2014.a concept paper was received
6、 from pqtinspections for a proposed structure of a new guidance document which was discussed in detail.the concept paper consolidated existing normative principles and gave some illustrative examples on their implementation.in the appendix to the concept paper extracts from existing good practices a
7、nd guidance documents were combined to illustrate the current relevant guidance on assuring the reliability of data and related gxp matters.in view of the increasing number of observations made during inspections regarding data management practices the committee endorsed the proposal.following this
8、endorsement,a draft document was prepared by the colleagues from pqt-inspection and a drafting group,including national inspectors.this draft was discussed at a consultation on data management,bioequivalence,good manufacturing practices and medicines inspection held 29 june1 july 2015.a revised draf
9、t document was subsequently prepared by the authors,the drafting group,based on the feedback received during this consultation and the subsequent who workshop on data management.collaboration is being sort with other organizations towards future convergence in this area.this first draft is presented
10、 herewith for comments.1.introduction and background medicines regulatory systems worldwide have always depended upon the knowledge of organizations that develop,manufacture and package,test,distribute and monitor pharmaceutical products.implicit in the assessment and review process is a trust betwe
11、en the regulator and the regulated that the information submitted in dossiers and used in day-to-day decision-making is comprehensive,complete and reliable.data on which these decisions are based should therefore be complete as well as being accurate,legible,contemporaneous,original and attributable
12、;commonly referred to as“alcoa”.these basic alcoa principles and the related good practice expectations that assure data reliability are not new.much high-and mid-level normative guidance already【篇二:混凝土结构工程施工规范征求意见稿(最终稿)】请将你们发现的本规范中有关专利的内容和支持性文件随意见一并返回。中华人民共和国国家标准 national standard of p.r.china 混凝土结
13、构工程施工规范 code for construction of concrete structures (征求意见稿)(draft for comments)二九年五月 国家标准混凝土结构工程施工规范编制组声明 1本规范(征求意见稿)著作权为住房和城乡建设部所有。本规范尚未正式发布,任何单位不得以任何形式出版发行。任何单位或个人以经营为目的,以各种形式复制本规范(征求意见稿)的任何部分,必须事先征得国家标准混凝土结构工程施工规范编制组(以下简称本规范编制组)的书面同意。任何单位或个人将本规范(征求意见稿)的任何部分上传至网络用于传播,必须事先征得本规范编制组的书面同意。2本规范编制组原则上不
14、反对本规范中含有专利,但该专利应是本规范中难以替代的技术,且不存在其他拒绝涉及该专利的实质性理由。此处所称专利是指依据中华人民共和国专利法获得授权且处于保护期内的发明创造。本规范(征求意见稿)的内容不涉及任何参与本规范编制的组织或个人的专利。本规范(征求意见稿)编制过程中,本规范编制组尚未识别出涉及专利的内容。参与本规范编制的组织或个人知晓如下义务:对其所知悉的相关专利,应及时向本规范编制组提供专利信息及相应的证明材料。若认为本规范(征求意见稿)的某些内容可能涉及专利(含处于专利申请阶段尚未获得授权的发明创造),请将本规范中有关专利的内容和支持性文件送达本规范编制组。本规范编制组将请专利权利人
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