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Data Integrity in Pharmaceutical and Medical Devices Regulation Operations: Best Practices Guide to Electronic Records Compliance
October 21, 2016 by Productivity Press
数据可靠性在医药和医疗器械监管操作:电子记录的最佳实践指南
出版日期 : 2016年10月21日
372页
- 以实用的方式编写,以满足任何卫生机构的从业者的数据可靠性的要求
- 在良好制造实践环境中检查计算机系统的控制包括案例研究
- 提供一种实用的方法来提高效率,并确保正确实现数据可靠性控制的设计和测试

Contents
- Preface
- Introduction
- Inspection Trends
- Electronic Records Life Cycle
- MHRA Definitions
- Electronic Records Governance
- Relevant Electronic Records Management
-Procedural Controls
- Electronic Records Controls - Supporting Processes
- Electronic Records Controls - In Storage
- Electronic Records Controls - During Processing
- Electronic Records Controls - While in Transit
. Trustworthy Computer Systems
- Electronic Records and Service Providers
- Relevant Worldwide GMP Regulations and Guidelines
- MHRA Guidance
- Electronic Records Management - 21 CFR Part 211
- Electronic Records Management - EMA Annex 11
- Self Inspection
- Summary
- Appendices: Glossary of Terms
- Abbreviations and Acronyms
- Regulatory Cross Match
- MHRA GMP Data Integrity Definitions and Guidance for Industry March 2015
- Relevant Worldwide GCP and GLP Regulations and Guidelines
- Electronic Records Integrity in Non-Clinical Laboratories
- Electronic Records Integrity in Clinical Systems
- Electronic Integrity in a Data Warehouse and Business Intelligence.
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