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Ensuring the Integrity of Electronic Health Records
Af: Orlando Lopez Engelsk Paperback
SPAR
kr 73
Ensuring the Integrity of Electronic Health Records
Af: Orlando Lopez Engelsk Paperback

Data integrity is a critical aspect to the design, implementation, and usage of any system which stores, processes, or retrieves data. The overall intent of any data integrity technique is the same: ensure data is recorded exactly as intended and, upon later retrieval, ensure the data is the same as it was when originally recorded. Any alternation to the data is then traced to the person who made the modification. The integrity of data in a patient’s electronic health record is critical to ensuring the safety of the patient.

This book is relevant to production systems and quality control systems associated with the manufacture of pharmaceuticals and medical device products and updates the practical information to enable better understanding of the controls applicable to e-records. The book highlights the e-records suitability implementation and associated risk-assessed controls, and e-records handling. The book also provides updated regulatory standards from global regulatory organizations such as MHRA, Medicines and Healthcare Products Regulatory Agency (UK); FDA, Food and Drug Administration (US); National Medical Products Association (China); TGA, Therapeutic Goods Administration (Australia); SIMGP, Russia State Institute of Medicines and Good Practices; and the World Health Organization, to name a few.

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Data integrity is a critical aspect to the design, implementation, and usage of any system which stores, processes, or retrieves data. The overall intent of any data integrity technique is the same: ensure data is recorded exactly as intended and, upon later retrieval, ensure the data is the same as it was when originally recorded. Any alternation to the data is then traced to the person who made the modification. The integrity of data in a patient’s electronic health record is critical to ensuring the safety of the patient.

This book is relevant to production systems and quality control systems associated with the manufacture of pharmaceuticals and medical device products and updates the practical information to enable better understanding of the controls applicable to e-records. The book highlights the e-records suitability implementation and associated risk-assessed controls, and e-records handling. The book also provides updated regulatory standards from global regulatory organizations such as MHRA, Medicines and Healthcare Products Regulatory Agency (UK); FDA, Food and Drug Administration (US); National Medical Products Association (China); TGA, Therapeutic Goods Administration (Australia); SIMGP, Russia State Institute of Medicines and Good Practices; and the World Health Organization, to name a few.

Produktdetaljer
Sprog: Engelsk
Sider: 320
ISBN-13: 9780367616038
Indbinding: Paperback
Udgave:
ISBN-10: 0367616033
Kategori: Sundhedsvæsen
Udg. Dato: 22 dec 2020
Længde: 26mm
Bredde: 177mm
Højde: 253mm
Oplagsdato: 22 dec 2020
Forfatter(e): Orlando Lopez
Forfatter(e) Orlando Lopez


Kategori Sundhedsvæsen


Sprog Engelsk


Indbinding Paperback


Sider 320


Udgave


Længde 26mm


Bredde 177mm


Højde 253mm

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