May 23: Difference between revisions

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## At risk June 9
## At risk June 9
# White paper
# White paper
;Updated White Paper with content based on discussions of May 19-23 inclusive: [ftp://ftp.ihe.net/Quality/Technical_Comittee/2008/21_5_2008_IHE_QRPH_White_Paper_version1%5B1%5D.doc White paper]
## Updated White Paper with content based on discussions of May 19-23 inclusive: [ftp://ftp.ihe.net/Quality/Technical_Comittee/2008/21_5_2008_IHE_QRPH_White_Paper_version1%5B1%5D.doc White paper]
## Requires 2 calls
## Requires 2 calls

Revision as of 12:12, 23 May 2008

May 23 QRPH Face-to-Face Meeting Minutes

Attendees:

  • Floyd Eisenberg (Siemens)
  • Jason Colquit (Greenway Medical Systems)
  • Sheila Teasdale (AMA)
  • Delane Heldt (AMA)
  • Harry Solomon (GE)
  • Patty Craig (Joint Commission)
  • Jan Orton (Intermountain Healthcare)
  • Randolph Barrows (MedAllies)
  • Daemon Whittenberg (Greenway Medical Systems)
  • Joann Larson (Kaiser)
  • Ana Estelrich (GMP-DIP)
  • Chris Carr (RSNA)
  1. Clinical Research Profile
    1. “Other option” requires review – Send to QRPH TC – Schedule one call
  2. Drug Safety Profile
    1. Pull content from Clinical Research Profile
    2. E2B describes data elements
      1. How to describe what was the adverse event
      2. Need to identify the information to be send and how based on the trigger
    3. Calls
    4. At risk June 9
  3. White paper
    1. Updated White Paper with content based on discussions of May 19-23 inclusive: White paper
    2. Requires 2 calls