Difference between revisions of "HL7 Stability Standard Implementation Guide Teleconference Minutes 2011-01-24"

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(Created page with "==HL7 Stability Standard Pilot/Implementation Guide Teleconference Minutes== '''January 24, 2011''' Attendees: Norman Gregory (CVM), David Longstaff (CVM), Tim Lee (CBER), Cath...")
 
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Norman Gregory (CVM), David Longstaff (CVM), Tim Lee (CBER), Catherine Hosage-Norman (Sunovion), Mike Yang (ScienTek Software), Edward Pec (Abbott Laboratories), Jennifer Rice (Alpharma), and Sandra Spiewak (Reed Technology and Information Services Inc.)
 
Norman Gregory (CVM), David Longstaff (CVM), Tim Lee (CBER), Catherine Hosage-Norman (Sunovion), Mike Yang (ScienTek Software), Edward Pec (Abbott Laboratories), Jennifer Rice (Alpharma), and Sandra Spiewak (Reed Technology and Information Services Inc.)
  
*Attached is an e-mail from Art Griesser with question about SPL schematron rules and/or the schematron implementation used for SPL along with a pdf file about schematron implementations.  I did forward the e-mail to the FDA SPL people and to the SPL schematron developer.  If you use SPL or are familiar with schematron please take a look at the e-mail and respond if you know the answer to any of the questions.   
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*The attached e-mail from Art Griesser (http://gforge.hl7.org/gf/download/docmanfileversion/6111/7978/E-Mail.doc) with question about SPL schematron rules and/or the schematron implementation used for SPL along with a pdf file (http://gforge.hl7.org/gf/download/docmanfileversion/6112/7979/schematron_implementations.pdf) about schematron implementations.  I did forward the e-mail to the FDA SPL people and to the SPL schematron developer.  If you use SPL or are familiar with schematron please take a look at the e-mail and respond if you know the answer to any of the questions.   
 
*Attached is the validation document (HL7 Drug Stability Reporting Validation Procedures (1-24-11).doc) which has all the edited and revised information from the elements (1-24-11).doc inserted in Section 1.3 Document information.  Once we are satisfied with the information in this section we will look at the total document.
 
*Attached is the validation document (HL7 Drug Stability Reporting Validation Procedures (1-24-11).doc) which has all the edited and revised information from the elements (1-24-11).doc inserted in Section 1.3 Document information.  Once we are satisfied with the information in this section we will look at the total document.
  

Revision as of 14:32, 25 January 2011

HL7 Stability Standard Pilot/Implementation Guide Teleconference Minutes

January 24, 2011

Attendees:

Norman Gregory (CVM), David Longstaff (CVM), Tim Lee (CBER), Catherine Hosage-Norman (Sunovion), Mike Yang (ScienTek Software), Edward Pec (Abbott Laboratories), Jennifer Rice (Alpharma), and Sandra Spiewak (Reed Technology and Information Services Inc.)

  • The attached e-mail from Art Griesser (http://gforge.hl7.org/gf/download/docmanfileversion/6111/7978/E-Mail.doc) with question about SPL schematron rules and/or the schematron implementation used for SPL along with a pdf file (http://gforge.hl7.org/gf/download/docmanfileversion/6112/7979/schematron_implementations.pdf) about schematron implementations. I did forward the e-mail to the FDA SPL people and to the SPL schematron developer. If you use SPL or are familiar with schematron please take a look at the e-mail and respond if you know the answer to any of the questions.
  • Attached is the validation document (HL7 Drug Stability Reporting Validation Procedures (1-24-11).doc) which has all the edited and revised information from the elements (1-24-11).doc inserted in Section 1.3 Document information. Once we are satisfied with the information in this section we will look at the total document.

Agenda for January 31, 2011 Teleconference:

  • We will continue to use Adobe connect (to join the meeting: https://collaboration.fda.gov/hl7/).
  • Schematron progress update
  • eStability Validation Procedures document and element document.