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- W8147918 abstract "This chapter begins with a section on the regulation of clinical computing, which describes the primary legislation and standards covering the use of a computer (either hardware or software) as a clinical device. The two major regulators, the MHRA and FDA, are described before moving on to regulatory standards. The IEC 601 family, the Medical Devices Directive, CE marking, IEC 80001-1 are discussed, followed by the major legislation: the Data Protection Act and the Freedom of Information Act. This section on data security requirements describes both “standard” best practices, and healthcare-related additions/amendments. The prevention of unauthorized access is considered first, via firewalls, anti-virus measures, encryption (including PGP), and access control. Secondly, resilience is investigated via replication, backup, and archiving before turning our attention to network bandwidth and infrastructure. Finally, information governance is described, including the NHS statement of compliance. This final section in the chapter covers data communication and exchange through standards and protocols such as Digital Imaging and Communications in Medicine (DICOM) and Health Level Seven (HL7). Finally, the links to an Electronic Patient Record via interfaces are considered, together with the e-Government Interoperability Framework." @default.
- W8147918 created "2016-06-24" @default.
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- W8147918 date "2014-01-01" @default.
- W8147918 modified "2023-09-24" @default.
- W8147918 title "Information Communications Technology" @default.
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- W8147918 doi "https://doi.org/10.1016/b978-0-12-396961-3.00008-1" @default.
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