FDA没有专门针对计算机化系统验证的指南,只有在法规中要求计算机化系统应该验证,和计算机化系统相关的指南只有Computerized Systems Used in Clinical Investigations和Class II Special Controls Guidance Document: Computerized Labor Monitoring Systems,针对计算机化系统中电子数据的要求的文件主要有下面三个:
21CFR Part11 ELECTRONIC RECORDS; ELECTRONIC SIGNATURES
FDA Guidance for Industry:Part 11, Electronic Records; Electronic Signatures — Scope and Application
FDA Guidance for Industry:FDA Data Integrity and Compliance With CGMP