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HITSP C151 Clinical Research Document Component V1.0 25 Jan 2010


Type:Data Agreement
Start Date:2010-01-25
Scope:1.1 OVERVIEW : The Healthcare Information Technology Standards Panel (HITSP) Clinical Research Document (CRD) Component describes the content and format to be used for pre-population data within the Retrieve Form Transaction described within the IHE Retrieve Form for Data-Capture (RFD) Integration Profile. HITSP supports RFD through HITSP/TP50 Retrieve Form for Data Capture.

The purpose of the CRD Component is to support a standard set of data in the HL7 Continuity of Care Document (CCD) format which the Form Filler provides for use in Clinical Research. In addition this profile will reference the ability to convert this output into a standard case report form (Standard CRF) based on the Clinical Data Acquisition Standards Harmonization (CDASH) specification and the Operational Data Modal (ODN) of Clinical Data Interchange Standards Consortium (CDISC).
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is composed of HITSP C151 Rules for Implementing/Data Mapping   

There are no Value Domains linked to HITSP C151 Clinical Research Document Component V1.0 25 Jan 2010.

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