• An incident response plan detailing responsibilities and how to react and
recover from incidents, shall be in place. Staff involved in the incident
response plan shall be trained to respond appropriately and effectively.
• A formal user provisioning and de-provisioning process shall be
implemented to enable the appropriate management of access rights to
medical devices.
• Users shall be assigned unique accounts to medical devices.
• User access rights to medical devices shall be reviewed for appropriateness
and corrected as needed, at regular intervals not exceeding once a year.
48
| Crystal-M Imager | Introduction
3852B EN 20210601 1655
Содержание 5367/300
Страница 1: ...Crystal M Imager 5367 300 User Manual 3852B EN 20210601 1655 ...
Страница 12: ...12 Crystal M Imager Crystal M Imager 3852B EN 20210601 1655 ...
Страница 57: ... The display Crystal M Imager Introduction 57 3852B EN 20210601 1655 ...
Страница 89: ...WARNING Never reuse a jammed film Crystal M Imager Basic Operation operator mode 89 3852B EN 20210601 1655 ...
Страница 128: ...5 Press the OK button on the touchscreen 128 Crystal M Imager Preventive maintenance schedule 3852B EN 20210601 1655 ...
Страница 134: ... Cables transducers and accessories 134 Crystal M Imager Remarks for HF emission and immunity 3852B EN 20210601 1655 ...
Страница 152: ...4 18 2832E EN 20151008 5 Remove plastic bag 152 Crystal M Imager Plug Play Installation Manual 3852B EN 20210601 1655 ...
Страница 161: ...Crystal M Imager Plug Play Installation Manual 161 3852B EN 20210601 1655 ...