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Federal Agencies must use the Recognized Interoperability Standards that have been harmonized by HITSP.
Component
C 37 - HITSP Lab Report Document Component
The Lab Report Document Component prescribes the use of the standard Clinical Document Architecture Release 2 (CDA R2), as in the HL7 V3 2006 normative edition profiled by IHE LAB TF-3 for: transmission of complete, preliminary, final and updated laboratory results to the EHR system (local or remote) of the ordering clinician; transmission of complete, preliminary, final and updated (or notification) to the EHR system (local or remote) or other clinical data system of designated providers of care (with respect to a specific patient); transmission of laboratory result data from electronically enabled healthcare delivery and public health systems in standardized and anonymized format to authorized Public Health Agencies with less than one day lag time.
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Construct
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Referenced by
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C 37
HITSP Lab Report Document Component
Version:2.0
IS 1 V:2.1
IS 2 V:2.1
IS 3 V:3.0
IS 5 V:1.0
Recognized
DOWNLOAD
C 37
HITSP Lab Report Document Component
Version:2.1
IS 2 V:3.0
IS 1 V:3.0
Recognized
DOWNLOAD
C 37
HITSP Lab Report Document Component
Version:2.2
IS 2 V:3.1
IS 3 V:3.1
IS 5 V:1.1
IS 11 V:0.0.2
IS 3 V:3.1.2
IS 4 V:1.2.2
IS 2 V:3.1.1
IS 5 V:1.1.2
IS 9 V:0.0.2
IS 8 V:0.0.2
IS 3 V:3.1.1
IS 5 V:1.1.1
IS 8 V:0.0.1
IS 9 V:0.0.1
Recognized
DOWNLOAD
C 37
HITSP Lab Report Document Component
Version:2.3
IS 1 V:3.1
IS 2 V:3.2
IS 3 V:4.0
IS 4 V:2.0
IS 5 V:2.0
IS 8 V:1.0
IS 9 V:1.0
IS 11 V:1.0
Recognized
DOWNLOAD
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