CDA R2.0 Vs Clinical Statement vs RIM Acts

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Presentation transcript:

CDA R2.0 Vs Clinical Statement vs RIM Acts CDA R2.1 –ACTS CDA R2.0 Vs Clinical Statement vs RIM Acts

ACT CDA R2.0 Clinical Statement RIM

Observation CDA R2.0 Clinical Statement RIM

Procedure CDA R2.0 Clinical Statement RIM

Substance Administration CDA R2.0 Clinical Statement RIM

Supply CDA R2.0 Clinical Statement RIM

Encounter CDA R2.0 Clinical Statement RIM

Organizer CDA R2.0 Clinical Statement RIM

Observation Range CDA R2.0 Clinical Statement RIM

Criterion CDA R2.0 Clinical Statement RIM

External Acts CDA R2.0 Clinical Statement RIM

CDA R2.0 Vs Clinical Statement vs RIM Acts CDA R2.1 – Other CDA R2.0 Vs Clinical Statement vs RIM Acts

Manufactured Product CDA R2.0 Clinical Statement RIM Omit contextControlCode as it adds additional complexity Our default assumption is that contextControlCodes when not Identified are assumed to be set to “ON” For generic Partisipant the typeCodes Need to match to enable “OP”

Manufactured Product CDA R2.0 Clinical Statement RIM

Manufactured Product CDA R2.0 Clinical Statement

Participant CDA R2.0 Clinical Statement RIM

Performer CDA R2.0 Clinical Statement RIM

Participant / Performer CDA R2.0 Clinical Statement RIM

Participant / performer CDA R2.0 Clinical Statement RIM

Specimen CDA R2.0 Clinical Statement RIM

Specimen CDA R2.0 Clinical Statement RIM

Specimen CDA R2.0 Clinical Statement RIM

UDI Considerations Unique Device Identifier: Device Identifier - code Manufacture date Expiration date Lot number Serial number One field for two uses DIN - Donation Identifier Number DIC - Distinct identification code

Observation Range & Criterion Clinical Statement