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 regulatory compliance within the context of quality assurance. He demonstrates the importance of integrating validation activities into the system lifecycle using a structured top-down approach. He covers practical applications of quality assurance and engineering techniques as they relate to the development of systems fit to meet user and regulatory requirements.
發表於2024-12-11
21 CFR Part 11 2024 pdf epub mobi 電子書 下載
圖書標籤: 美國 法律 參考資料 Signatures IT Electronic
21 CFR Part 11 2024 pdf epub mobi 電子書 下載