Minutes QRPH Drug Safety Content Profile July 17, 2008

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Agenda (Minutes) QRPH Drug Safety Content Profile July 17, 2008

Attendees

  • Floyd Eisenberg, Siemens Healthcare (Co-chair)
  • Ana Estelrich, DIP, GMP (Planning Committee Co-Chair)
  • Landen Bain, CDISC
  • Patty Craig, The Joint Commission
  • Shawn Dunaway-Shanks, Siemens Healthcare
  • Thomas Kuhn, ACP
  • Shirley Neal, Misys
  • Rhonda Facile, CDISC
  • Jacob Reider, Misys
  • Lisa Spellman, HIMSS
  • Mick Talley, University Bank
  • Gary Walker, Quintiles

Drug Safety Content

Prior Discussions for Reference:

Discussion

  • Agenda for face-to-face meeting reviewed Agenda_QRPH_July_22-25_Meeting
  • Notification of Collaborative for Performance Measure Integration with EHRS on Monday, July 21 in Oakbrook to coordinate with QRPH meeting to start on Tuesday, July 22
  • Overview of content for Drug Safety Reporting Content White Paper
    • No new information to add on today's call
    • Volunteers agreed to contact others to provide current state for use cases of clinical trials and phas IV trials
    • Volunteer to update CDASH data elements in table by next Wednesday
    • Suggestion to include discussion about BRIDG and incorporate input from HL7 RCRIM Technical Committee
  • Performance Measurement White Paper comments received to date reviewed in total. Proposed resolution of current comments updated to Excel spreadsheet now posted at White Paper Comment Spreadsheet
  • Lisa Spellman provided projected publication dates for IHE work product - July 30, August 5, August 12. Thus far, current work products from QRDA out for comment are on track for completion next week. Anticipate July 30 publication. Drug Safety White Paper will likely take more time.

Next Steps

Return to: Quality, Research and Public Health Technical Committee

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