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[资源分享] 已更新—WHO TRS(技术报告丛书)及ECSPP、PQ(预认证)现行链接与信息分享

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药士
发表于 2022-5-13 11:04:04 | 显示全部楼层 |阅读模式

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本帖最后由 JimmyHE8888 于 2022-5-13 11:37 编辑

如题,之前很多人知道WHO TRS的内容,是从PUBLICATIONS(即出版物)分项。然而从2021年WHO发布TRS 1033开始,相关TRS的内容已经重新划归了分项,即重新归类到ECSPP(药物制剂标准专家委员会)项下,当然最新发布的也会在IRIS出版物栏目中提示。

总体来说,一共有几种途径可以获取到跟WHO ECSPP发布的TRS相关资料的途径,分享如下——


感觉有用的话,千万不要吝惜你给个专业小红心,这将对我有极大的鼓励。谢谢。





1) ECSPP (
Expert Committee on Specifications for Pharmaceutical Preparations   )  直接相关页面


https://www.who.int/teams/health-product-and-policy-standards/standards-and-specifications/norms-and-standards-for-pharmaceuticals/expert-committee-on-specifications-for-pharmaceutical-preparations   


里面有关于ECSPP(药物制剂标准专家委员会)的介绍——
About the Expert Committee

An Expert Committee is the highest official advisory body to the Director-General of WHO as well as to all the Organization’s Member States. An Expert Committee is established by the WHO World Health Assembly (WHA) or by an Executive Board decision.

Rules of procedure

WHO Expert Committees are governed through specific rules of procedure. The Regulations for Expert Advisory Panels and Committees can be found in the WHO Basic Documents. More importantly, they can be found in the Constitution of the World Health Organization.  Reference is made to Expert Committees in Chapter V, Article 18, as well as in Chapter VIII, Articles 38-40. In addition to the Constitution of the of the World Health Organization, regulations for Expert Advisory Panels and Committees are also included in a special annex entitled Rules of Procedure for Expert Committees in the Regulations for Expert Advisory Panels and Committees.



同样,也有TRS(Technical Report Series,即技术报告丛书)的链接,包括2021年3月分布的TRS1033(目前最新版),以及自1969年起发布的相关TRS。请注意,这里看见的TRS都是正文与附件合为一个PDF的完整版本。

从新闻公告来说,2022年4月25日-5月2日,ECSPP召开了新一轮的线上会议,讨论一些列工作,因此可以推测,下一版的TRS可能也会在今年下半年或明年初发布。





2) 从药品预认证()网页
https://extranet.who.int/pqweb/medicines/WHOguidance-documents


进入相关WHO TRS指南汇总表
https://extranet.who.int/pqweb/medicines/who-technical-report-series
在该页面查找的TRS指南,则是已经预分了领域/种类,而且是从原TRS中提取的附件,因此可以单独使用



感觉有用的话,千万不要吝惜你给个专业小红心,这将对我有极大的鼓励。谢谢。


WHO ECSPP-Webpage-2.png
WHO PQT-Guidance TRS-1.png
WHO ECSPP-Webpage-1.png
WHO PQT-Guidance.png
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药士
 楼主| 发表于 2022-5-13 11:25:05 | 显示全部楼层
自2020年10月起,WHO预认证(PQ)小组做了职责调整,将药品预认证、疫苗、IVD(诊断试剂)、VCP(媒介控制产品,例如蚊帐、杀虫剂等)、免疫装置等项目合并到一个大框架下。
此外,一个与以往的预认证网站不同的点是将INSPECTION SERVICES(检查服务)单独拎出来,包含相关服务的使命、过程与要求、输出报告及历史归档等,这样更方便除了申请者(即生产商或QC实验室)、采购机构与不同国家的官方监管机构进行有关信息的检索与参考。





而且把网站页做了整合升级—— https://extranet.who.int/pqweb/





下面复制一些WHO PQ的历史与使命,附件放了一个2019年发布的WHO PQ的影响评估,供参考。



History and Mission of WHO Prequalification


Today, we have prequalified almost 1,500 products — in vitro diagnostics (IVDs), male circumcision devices, medicines, vaccines, immunization devices and cold chain equipment, and vector control products — that have assisted in improving public health in low- and middle-income countries (LMIC). WHO prequalification has become a trusted and reputed symbol for safety, quality and efficacy across stakeholders.
What types of product does WHO prequalify?
IVD prequalification covers a wide array of diagnostics for both endemic and epidemic diseases in LMIC.
Medicines prequalification currently covers HIV/AIDS, malaria, TB, reproductive health, hepatitis, diarrhoeal diseases and selected neglected tropical diseases. It recently intiated prequalification of biotherapeutic products: selected products to treat certain types of cancer, and human insulin for diabetes.
Vaccines prequalification covers all vaccines required for routine immunization against 24 priority diseases, while immunization devices prequalification covers all equipment needed for an effective national vaccine programme.
Vector control prequalification is the "newest" prequalification product stream, focusing on assessment of new products used for the prevention of vector-borne disease. Products assessed include bed nets, sprays and larvicides.
What difference does WHO prequalification make?
Assessment of WHO-prequalification impact has demonstrated that:
  • it has enabled a large donor-funded market size of approximately US$ 3.5 billion of quality, safe and effective IVDs, medicines and vaccines: it is likely that, in addition, prequalified IVDs, medicines and vaccines are procured by national governments, as well as private-sector organizations within country
  • helps ensure that products are developed for an LMIC context: meaning that they are appropriate for use in the populations for which they intended and are not negatively affected by the conditions of the environment in which they may be transported or stored
  • plays an important role in guiding product innovation and early-stage development: examples have included bringing paediatric TB products to market in sub-Saharan Africa and promulgating the deployment and use of HIV self-testing diagnostics
  • it has helped raised manufacturing standards in LMIC: the number of medicines and vaccines MIC manufacturers participating successfully in WHO prequalification continues to grow: meaning that capacity and confidence with respect to LMIC production of quality-assured products in those countries is likewise growing; LMIC now represent more than 40% of all manufacturers with prequalified medicines and 50% of manufacturers with prequalified vaccines.
In addition, WHO prequalification has contributed to strengthening of country health and regulatory systems. This has included work in support of WHO's development of norms and standards, its contribution to strengthening of national regulatory authorities and regulatory harmonization, and its support to building national and global capacity for safety monitoring and vigilance for health products.
The public health impact of prequalification is considerable. In 2019 it was estimated that about 400 million additional patients may have obtained access to needed health products on an annual basis thanks to generation of savings by WHO prequalification (and assuming that funding is not diverted to other causes). In other words, WHO prequalification is a sound investment. Working in collaboration with many stakeholders, in the broad ecosystem that is global health, WHO prequalification contributes to savings of approximately US$ 30–40 for every US$ 1 that is invested in it.
In addition: risk-based assessment
WHO prequalification also undertakes risk-based assessment of products during public health emergencies of international concern. This has included for the Ebola and Zika virus disease, and most recently for coronavirus disease (COVID-19). Risk-based assessment is also carried out on behalf of procurement agencies when prequalified or stringently-approved products are yet available or not availabe in sufficient quantity.










WHO PQT Homepage.png

Impact-assessment_WHO-PQ-Reg-systems.pdf

2.75 MB, 下载次数: 104

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药徒
发表于 2022-5-13 15:58:50 | 显示全部楼层
不错不错,小红心奉上
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药徒
发表于 2022-5-13 16:30:02 | 显示全部楼层
JimmyHE8888 发表于 2022-5-13 11:25
自2020年10月起,WHO预认证(PQ)小组做了职责调整,将药品预认证、疫苗、IVD(诊断试剂)、VCP(媒介控制 ...

谢谢分享                     
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发表于 2022-5-13 18:43:16 | 显示全部楼层
我想要中文版的
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药生
发表于 2022-5-13 19:08:01 | 显示全部楼层
非常感谢,辛苦了!
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药徒
发表于 2022-5-14 19:59:37 | 显示全部楼层
.谢谢各位老师的分享。
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药生
发表于 2022-5-14 21:59:37 | 显示全部楼层
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药徒
发表于 2022-5-15 11:08:30 | 显示全部楼层
JimmyHE8888 发表于 2022-5-13 11:25
自2020年10月起,WHO预认证(PQ)小组做了职责调整,将药品预认证、疫苗、IVD(诊断试剂)、VCP(媒介控制 ...

谢谢分享,多读多学
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药徒
发表于 2022-5-17 10:18:02 | 显示全部楼层
必须奉上小红心
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药徒
发表于 2022-5-17 12:38:06 | 显示全部楼层
请问一下,除了技术汇报系列,指南系列是在哪里发布的,比如激素类药物的指南,是什么形式发布的呢?
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药士
 楼主| 发表于 2022-5-17 15:06:02 | 显示全部楼层
HIDIC 发表于 2022-5-17 12:38
请问一下,除了技术汇报系列,指南系列是在哪里发布的,比如激素类药物的指南,是什么形式发布的呢?

从理论上来说,我这个帖子里分享的TRS,仅仅是针对药品类/药物制剂。
如果是其他领域,例如疾病(包括流行病、紧急状况等 )、健康、烟草控制等等都是有不同的专家委员会,每年的集中会议探讨指南或更新之后都会有相应报告,所以这也是为什么帖子里的链接与TRS编号其实不是连续的,因为给ECSPP相关分配的序号正好是所见而已。

一些特定产品(例如激素),我的个人建议是先在WHO主站上检索项目或疾病治疗谱的内容,再看是否有详细解读。

我到时有空也再去WHO的官网看看,因为曾有相当长一段时间工作接触比较多就是ECSPP与WHO PQ的内容。

点评

谢谢。  详情 回复 发表于 2022-5-17 17:41
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药徒
发表于 2022-5-17 17:41:04 | 显示全部楼层
JimmyHE8888 发表于 2022-5-17 15:06
从理论上来说,我这个帖子里分享的TRS,仅仅是针对药品类/药物制剂。
如果是其他领域,例如疾病(包括流 ...

谢谢。
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药徒
发表于 2022-5-18 07:59:16 | 显示全部楼层
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药徒
发表于 2022-5-19 10:09:40 | 显示全部楼层
楼主好心人,祝一切顺利
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发表于 2022-5-19 12:39:33 | 显示全部楼层
不错不错,小红心奉上
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药士
 楼主| 发表于 2022-5-19 17:35:10 | 显示全部楼层
本帖最后由 JimmyHE8888 于 2022-5-19 17:36 编辑

如果需要无专题查询WHO官方发布的最新出版物,也可以通过IRIS(Institutional  Repository for Information Sharing,即”信息共享数据库“)的文献库网页进行浏览
在一楼中也提到过,假若WHO方面通过ECSPP的审批,则最新版的与药品/制剂相关的TRS也会收纳发布在该页面,所以也是可以做相关检索的一种途径。

IRIS的主页——
https://apps.who.int/iris


语言快速链接(或通过网页右上角语言选项切换),貌似该页面可以智能识别用户所在区域的优先语言(当然,也不排除可能是浏览器的设置,大家自己尝试一下)

https://apps.who.int/iris/?locale-attribute=en& (英文页面)
https://apps.who.int/iris/?locale-attribute=zh& (中文页面,但是发布的出版物依然是英文版,除非官方有翻译版










WHO IRIS Homepage-English.png
WHO IRIS主页-中文.png
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药徒
发表于 2022-5-20 09:50:54 | 显示全部楼层
必须认可                          
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药神
发表于 2022-7-4 19:25:25 | 显示全部楼层
好资料,学习借鉴
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药徒
发表于 2022-7-5 16:19:00 | 显示全部楼层
谢谢楼主,怎么找到TRS1004 lQLPJxZ2iuLVCefNAq7NAhaw_vBZQRApu18Cw0lQOoBUAA_534_686.png

点评

向下点击打开折叠的目录菜单,就有你图中那些材料的英文原版了,迅雷或者右键另存为保存即可,一般是PDF文件或者MS WORD格式的。 [attachimg]676325[/attachimg]  详情 回复 发表于 2022-7-7 08:54
从你的截图来看,这个应该是疫苗预认证的相关领域,可以从新的WHO PQ网站,进入PRODUCT STREAMS为VACCINES(疫苗)的下拉菜单,选择GUIDANCE DOCUMENTS(指南文件)[attachimg]676322[/attachimg] 点击图中左侧的  详情 回复 发表于 2022-7-7 08:50
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