CDA Management Group

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 life-cycle. 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.

Governance Documents

• Mission and Charter
• DMP
• eVoting
• GOM
• ANSI Essential Requirements

CDA Management Group Terms

If you have an issue that the CDA Management Group needs to address, you can log it to the JIRA for CDA_MG. Issues that need to be addressed by the CDA Management Group

• Create a new issue

The CDA-MG will focus its energy on enabling and ensuring the following:

• CDA development is coordinated and consistent across the organization and of high quality
• Work groups have timely feedback and guidance and their development of CDA products are aligned with the broader goals of HL7 and its constituent communities
• Work groups act in a coordinated manner with quick resolution of CDA related disputes
• Work groups understand what is expected of them and have access to the skills and tools necessary to perform their domain specific CDA related work
• Known Product Family risks are recorded, managed, and reviewed regularly per the SGB precept on vitality assessment.

• C-CDA Sample Document Registry
• C-CDA Value Set Expansions Package Registry
• CDA IG Publishing
• CDA Management Group and IAT Support
• CDA Package Review Process
• CDA Quality Plan Development
• Collaborative Template Review Project Pilot
• Improve Master Grid Product Page
• JIRA for CDA Specification Feedback
• Maturity Model for CDA Templates
• Test