550,88 €
612,09 €
-10% with code: EXTRA
21 Cfr Part 11
21 Cfr Part 11
550,88
612,09 €
  • We will send in 10–14 business days.
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 l…
612.09
  • Publisher:
  • ISBN-10: 084932243X
  • ISBN-13: 9780849322433
  • Format: 18.3 x 26.1 x 2 cm, kieti viršeliai
  • Language: English
  • SAVE -10% with code: EXTRA

21 Cfr Part 11 (e-book) (used book) | Orlando López | bookbook.eu

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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.

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  • Author: Orlando López
  • Publisher:
  • ISBN-10: 084932243X
  • ISBN-13: 9780849322433
  • Format: 18.3 x 26.1 x 2 cm, kieti viršeliai
  • Language: English English

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.

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