Difference between revisions of "Medical Product Information (SPLr5)"
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* [http://wiki.hl7.org/images/8/8d/SPLr4_to_SPL(r5)_presentation_04062010.pdf SPL R4 to R5 presentation -- May 6, 2010.] | * [http://wiki.hl7.org/images/8/8d/SPLr4_to_SPL(r5)_presentation_04062010.pdf SPL R4 to R5 presentation -- May 6, 2010.] | ||
| − | + | ===HL7 October Working Group Meeting October ballot | |
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| + | '''Structured Product Labeling (SPL5) Implementation Guide ballot results:''' | ||
* [http://wiki.hl7.org/images/d/d2/SPLr5_IGv1.0_-_new.pdf New SPL R5 Implementation Guide] | * [http://wiki.hl7.org/images/d/d2/SPLr5_IGv1.0_-_new.pdf New SPL R5 Implementation Guide] | ||
| − | New SPL IG compare to previous revision: | + | '''New SPL IG compare to previous revision:''' |
| − | http://wiki.hl7.org/images/3/3f/Compare_-_SPLr5_IGv1.0_-_new.pdf | + | |
| + | [http://wiki.hl7.org/images/3/3f/Compare_-_SPLr5_IGv1.0_-_new.pdf SPL R5 Implementation Guide compared to previous revision] | ||
==HL7 Ballot Materials - May 2010== | ==HL7 Ballot Materials - May 2010== | ||
Revision as of 13:48, 10 October 2010
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Contents
Project Scope
The project will extend the SPL model to develop a message that will allow transmission of a regulatory product information submission (labelling, listing, registration, unique device identifier and associated attributes) as specified by the Global Harmonization Task Force (GHTF) ad-hoc working group on (UDI.) submissions. The project will further provide references to other standards and external terminology resources required to populate the data elements defined in the standard. The work is based on existing work efforts: ISO/TC 215/SC WG6 N 547 (Health Informatics: IS#11615 Identification of Medicinal Products – Data Elements and Structure for the exchange of product information for drug dictionaries) and HL7 Structured Product Labeling and GHTF. This project will revise SPLr4 to leverage the data elements defined in the Common Product Model and reduce the SPL standard to the description of Header and Text information.
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Leadership
SPL Chair: Terry Brunone, theresa.m.brunone@gsk.com
Project Facilitator: Myron Finseth, 763-526-3071, myron.finseth@medtronic.com
Domain Expert: Terrie Reed, terrie.reed@fda.hhs.gov
Domain Expert: Anie Mathews, anie.mathews@fda.hhs.gov
Domain Expert: Jackie Elkin, jackie.elkin@medtronic.com
Modeling Facilitator: Gunther Schadow, gunther@pragmaticdata.com
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Project Team Participation
- First meeting is schedule for May 6, 2010
- Meetings occur every other Thursday, 10:30 eastern
- Telecom: 770-657-9270 . Passcode: 745896
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SPLr5 Project Meeting Minutes
Teleconference August 26, 2010
SPLr5 Project Working Documents
===HL7 October Working Group Meeting October ballot
Structured Product Labeling (SPL5) Implementation Guide ballot results:
New SPL IG compare to previous revision:
SPL R5 Implementation Guide compared to previous revision
HL7 Ballot Materials - May 2010
- Medical Product Information (includes Drugs, Devices, Biologics, Veterinary Products) (SPLr5) - Go to Regulated Products / Structure Product Labeling (SPL)
- Common Product Model - Go to Regulated Products / Common Product Model
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HL7 Voting Introduction
or
- HL7 Voting Background - Part 1
- HL7 Voting Ballot Desktop - Part 2
- HL7 Voting Understanding the Ballot Materials - Part 3
- HL7 Voting Casting Ballot - Part 4
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Overall Project Timeline (subject to change)
May 2010 – Project standards go to Ballot
- Medical Product Information (SPLr5) DSTU
- Common Product Model R10 DSTU
Oct 2010 – Project standards go to Ballot
- Medical Product Information (SPLr5) DSTU
- Common Product Model R10 DSTU
Jan 2011 – Project standards go to Ballot
- Medical Product Information (SPLr5) DSTU
- Common Product Model R10 DSTU
May 2011 – Project standards go to Ballot
- Medical Product Information (SPLr5) Normative
- Common Product Model R10 Normative
