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The Standards Governance Board (SGB), in conjunction with the Product Line Architecture Group (PLA), is in the process of establishing a new Clinical Document Architecture (CDA®) Product Family.
As part of that process, the SGB and PLA are seeking qualified HL7 members to form the Clinical Document Architecture Management Group (CDA-MG). To quote from the CDA-MG Mission and Charter, “The Clinical Document Architecture Management Group (CDA-MG) provides day-to-day oversight of the processes related to Clinical Document Architecture (CDA) products throughout their lifecycle. This includes ensuring CDA product quality, monitoring scope and consistency with Standards Governance Board (SGB) principles, and aiding in the resolution of CDA related intra- and inter-work group issues.” At this time, SGB seeks to represent a variety of perspectives on the CDA-MG including:
Members of the CDA-MG are appointed by the TSC based on recommendations from the SGB. We are currently seeking nominations (including self-nominations) for strong candidates. Desired skills
Nominations with a brief supporting paragraph outlining nominees' interests and experience should be sent to the SGB co-chairs: Paul Knapp and Austin Kreisler. Deadline to submit nominations: Friday, July 21, 2017. Questions? If you have any questions about the CDA-MG or the nominations, please contact Paul Knapp or Austin Kreisler. |
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Improving the quality of patient care through the effective sharing of clinical information among health care organizations, clinicians and their patients.