Difference between revisions of "Lessons from the HL7 Implementation Guide for CDA Release 2: Personal Healthcare Monitoring Report, Release 1"
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== Recommendation == | == Recommendation == | ||
Proposed additional information | Proposed additional information | ||
− | <br> | + | <br>'''Manufacturing info''': Serial number, Part number |
− | <br> | + | <br>'''Revisions''': Hardware revision, Software revision, Communication Protocol revision |
− | <br> | + | <br>'''Certifications''': Certification Authority and level of certification |
− | <br> | + | <br>'''Regulatory Status''': Regulated / unregulated and the regulatory authority |
Revision as of 17:06, 21 May 2010
Return to SDTC page; Return to CDA R3 Formal Proposals page.
See CDA R3 Formal Proposals for instructions on using this form. Failure to adhere to these instructions may result in delays. Editing of formal proposals is restricted to the submitter and SDTC co-chairs. Other changes will be undone. Comments can be captured in the associated discussion page.
(An announcement of this proposal must be submitted to the Structured Documents list to be formally submitted.)
Submitted by: <<Name>> | Revision date: 5/21/2010 |
Submitted date: 3/25/2010 | Change request ID: <<Change Request ID>> |
Issue
CDA needs a more detailed way to represent the device information in the playingDevice element. Currently, the CDA device information includes name, ID, manufacturerModelName, and softwareName.
Additional values for authoringDeice should also be considered.
Recommendation
Proposed additional information
Manufacturing info: Serial number, Part number
Revisions: Hardware revision, Software revision, Communication Protocol revision
Certifications: Certification Authority and level of certification
Regulatory Status: Regulated / unregulated and the regulatory authority
Rationale
Discussion
Recommended Action Items
Resolution
(Resolution is to be recorded here and in the referenced minutes, which are the authoritative source of resolution).