Abstract
This document presents an informative set of common, high-level security-related capabilities and additional considerations to be used across the entire life cycle of HEALTH SOFTWARE (including MEDICAL DEVICE software) and for the information exchange between the MEDICAL DEVICE MANUFACTURERS (MDMs), health software manufacturers, HEALTH DELIVERY ORGANIZATIONS (HDOs) and/or other stakeholders.
General information
-
Status: Under developmentStage: Close of comment period [30.60]
-
Edition: 1
-
Technical Committee :ISO/TC 215
- RSS updates
Life cycle
-
Previously
PublishedIEC/TR 80001-2-2:2012
PublishedIEC/TR 80001-2-8:2016
-
Now