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Requirement #

Description

1.2.1

The System shall have access to relevant patient medical data including diagnoses, medications, adverse events, radiology, labs, appointments, etc.

1.2.2

The System shall expose notification mechanisms (voicemail, pager, email, etc)  for use in creating knowledge modules.

1.2.3

The System shall enable providers to create, edit and store individual patient rules and workflows

1.2.4

The System shall provide (signal-processing) tools to automatically clean up noisy data such as self-reported medical device data delivered from non-institutional sources (e.g.: , home).  Clean up could include elimination of clear outliers.

1.2.5

The System shall enable providers to receive (optionally after automatic clean-up), edit and submit for final storage medical data delivered from non-institutional sources (e.g., home devices such as a scale or glucometer)

1.2.6

The System shall be capable of automatically executing individual patient rules and workflows on data received from non-institutional sources before physician review (event warning).

1.2.7

The System shall be capable of automatically executing individual patient rules and workflows on data received from non-institutional sources only after physician review (definitive warning).

1.2.8

To further generalize Requirements 1.2.6 and 1.2.7 above, the System shall provide a flexible and configurable workflow routing function. Example: direct to patient without provider review/approval, or only after provider review/approval, etc.

1.2.9

The System shall provide a secure capability for patient–provider email communication

1.2.10

The System shall provide patients with a self-appointing capability where they can book, cancel, and reschedule appointments.

1.2.11

The System shall provide justifications and references to be optionally returned with CDS recommendations for inclusion within notifications to recipients.