24小时热门版块排行榜

返回列表

1949stone

荣誉版主 (知名作家)

海纳百川

应助: 95 (初中生)
贵宾: 2.38
金币: 2332.6
散金: 3394
红花: 177
沙发: 8
帖子: 9855
在线: 2694.3小时
虫号: 765987
注册: 2009-05-08
性别: GG
专业: 药物分析
管辖: 分子生物

[交流] 非资源帖-做计算机系统验证的同志有福啦已有1人参与

CRC出版了EU Annex 11 Guide to Computer Validation Compliance for the Worldwide Health Agency GMP
http://www.crcpress.com/product/isbn/9781482243628
Features

Examines the implementation of computer systems compliance program based on EU Annex 11
Includes examples from laboratory, clinical, and manufacturing computer systems
Discusses electronic record integrity associated with stored information
Compares the Annex 11 with key worldwide computer systems regulations and guidelines, including U.S. Food and Drug Administration, Canada, Australia TGA, PIC/S, and China FDA

Summary

Good Manufacturing Practice (GMP) ensures medicinal products are produced consistently and controlled to the quality standards appropriate for their intended use and as required by product specifications or marketing authorization. Annex 11 details the European Medicines Agency (EMA) GMP requirements for computer systems.

The purpose of Annex 11 is to provide the EMA healthcare industry with consistent criteria for effective implementation, control, and use of computer systems. EU Annex 11 Guide to Computer Validation Compliance for the Worldwide Health Agency GMP supplies practical information to facilitate compliance with computer system GMP requirements, while highlighting and integrating the Annex 11 guidelines into the computer compliance program.

The ideas presented in this book are based on the author’s 25 years of experience with computer validation in the healthcare industry with various computer systems development, maintenance, and quality functions. The book details a practical approach to increase efficiency and to ensure that software development and maintenance are achieved correctly.

Examining the implementation of the computer systems validation entirely based on EU Annex 11, the book includes examples from laboratory, clinical, and manufacturing computer systems. It also discusses electronic record integrity associated with stored information.

回复此楼