ABSTRACT

Covering regulatory requirements stipulated by the FDA, this book delineates the organization, planning, verification, and documentation activities and procedural controls required for compliance with worldwide computer systems validation regulations. The author introduces supporting technologies such as encryption and digital signatures and places

chapter 1|4 pages

CH 1 Introduction

chapter 2|8 pages

CH 2 Validation Overview

chapter 5|4 pages

CH 5 Computer Validation Management Cycle

chapter 9|8 pages

CH 9 Inspections and Testing

chapter 10|24 pages

CH 10 Qualifications

chapter 11|4 pages

CH 11 SLC Documentation

part 12|2 pages

CH 12 Relevant Procedural Controls

chapter 13|4 pages

CH 13 Change Management

part 14|2 pages

CH 14 Training

chapter 15|12 pages

CH 15 Security

part 16|2 pages

CH 16 Source Code

chapter 18|6 pages

CH 18 Maintaining the State of Validation

chapter 19|4 pages

CH 19 Part 11 Remediation Project

chapter 20|4 pages

CH 20 Operational Checks

chapter 22|8 pages

CH 22 Electronic Records

chapter 23|4 pages

CH 23 Electronic Signatures

chapter 24|6 pages

CH 24 Technologies Supporting Part 111,2

chapter 25|6 pages

CH 25 All Together

chapter 26|4 pages

CH 26 The Future