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Ensuring the Integrity of Electronic Health Records

The Best Practices for E-records Compliance

Medium: Buch
ISBN: 978-0-367-61603-8
Verlag: Productivity Press
Erscheinungstermin: 22.12.2020
Lieferfrist: bis zu 10 Tage

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.


Produkteigenschaften


  • Artikelnummer: 9780367616038
  • Medium: Buch
  • ISBN: 978-0-367-61603-8
  • Verlag: Productivity Press
  • Erscheinungstermin: 22.12.2020
  • Sprache(n): Englisch
  • Auflage: 1. Auflage 2020
  • Produktform: Kartoniert
  • Gewicht: 645 g
  • Seiten: 340
  • Format (B x H x T): 178 x 254 x 18 mm
  • Ausgabetyp: Kein, Unbekannt

Themen


Autoren/Hrsg.

Autoren

1 Introduction 2 E-records Lifecycle Revisited 3 Data and E-records Lifecycles – A Comparison 4 MHRA Guidance – Revisited 5 E-records Integrity Expectations of EU GMP Inspectors 6 Comparison of Health Authorities E-records Integrity Expectations 7 Maxims of E-records Integrity 8 Vulnerabilities of E-records 9 CGMP E-records Risk Management 10 CGMP E-records Risk Assessments 11 Security Service 12 Defining and Managing Manufacturing Data 13 Controls on Transient Data 14 Digital Date and Timestamps 15 E-records Migration and Its Integrity 16 Ensuring E-records Integrity of Cloud Service Providers 17 E-records Integrity in Hybrid Systems 18 Technologies Supporting E-records Integrity 19 Integration Between Computer Systems and E-records Lifecycles 20 Miscellaneous E-records Integrity Issues 21 E-records Remediation Project Revisited – Medicine Manufacturing 22 Designing E-records Integrity into your Practices 23 Introduction to Data Quality 24 Summary