HL7 Stability Standard Implementation Guide Teleconference Minutes 2011-09-22

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HL7 Stability Standard Pilot/Implementation Guide Teleconference Minutes

September 22, 2011

Attendees:

Norman Gregory (CVM), Elizabeth Cormier (CVM), Catherine Hosage-Norman (Sunovion), Mike Mlodzik (Boehringer Ingelheim Vetmedica, Inc.), Mike Yang (ScienTek Software), Art Griesser (Promethues), and Howard Shatz (Data Conversion Laboratory, Inc.)

  • The Substance Type is fine the way we are doing it now.
  • The Product Type the displayName is mandatory and the the product name in the description is mandatory.
  • Code System version error from schematron will identify what version of the code system was used for the validation.
  • Storage has a code, StorageCondition does not have a code.
  • Is the container information in BatchIngredient mandatory? Catherine will test.
  • Need to think about getting away subset for codes or specify subset (ID would refer to subset, not complete file).
  • The IG every code element has to have an OID. IG and validation document need to be explicitly specific which OID is used when, not complete right now.
  • One of the product names has a TM in it, will not validate. The way we are handling product now it should not be a problem.
  • Need to set up a teleconference with the vocabulary people (FDA and NCI).

Agenda for September 26, 2011 Teleconference:

  • We will continue to use Adobe connect (to join the meeting: https://collaboration.fda.gov/hl7/)
  • Final changes to IG
  • Schematron progress update
  • eStabilty Validation Procedures document
  • Outstanding issues