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Data Integrity and Compliance - José Rodríguez-Pérez - Bog

Bag om Data Integrity and Compliance

Data integrity is a global mandatory requirement for the regulated healthcare industry. It is more than a mere expectation-it's a basic element of good documentation practices, one of the most fundamental pillars of a quality management system. Robustness and accuracy of the data submitted by manufacturers to regulatory authorities when bringing a medical product to market are crucial. The purpose of this book is to consolidate existing data integrity principles and expectations from several regulatory sources-including the U.S. Food and Drug Administration, World Health Organization, and European Medicines Agency-into a single and handy document that provides detailed, illustrative implementation guidance. It serves as a means of understanding regulatory agencies' position on good data management and the minimum expectation for how medical product manufacturers can achieve compliance.

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  • Sprog:
  • Engelsk
  • ISBN:
  • 9780873899871
  • Indbinding:
  • Hardback
  • Sideantal:
  • 274
  • Udgivet:
  • 8. maj 2019
  • Størrelse:
  • 157x19x235 mm.
  • Vægt:
  • 554 g.
  • 2-3 uger.
  • 18. januar 2025
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Forlænget returret til d. 31. januar 2025
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Beskrivelse af Data Integrity and Compliance

Data integrity is a global mandatory requirement for the regulated healthcare industry. It is more than a mere expectation-it's a basic element of good documentation practices, one of the most fundamental pillars of a quality management system. Robustness and accuracy of the data submitted by manufacturers to regulatory authorities when bringing a medical product to market are crucial.
The purpose of this book is to consolidate existing data integrity principles and expectations from several regulatory sources-including the U.S. Food and Drug Administration, World Health Organization, and European Medicines Agency-into a single and handy document that provides detailed, illustrative implementation guidance. It serves as a means of understanding regulatory agencies' position on good data management and the minimum expectation for how medical product manufacturers can achieve compliance.

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