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

2. ACT
CDA R2.0 Clinical Statement RIM

3. Observation
CDA R2.0 Clinical Statement RIM

4. Procedure
CDA R2.0 Clinical Statement RIM

5. Substance Administration
CDA R2.0 Clinical Statement RIM

6. Supply
CDA R2.0 Clinical Statement RIM

7. Encounter
CDA R2.0 Clinical Statement RIM

8. Organizer
CDA R2.0 Clinical Statement RIM

9. Observation Range
CDA R2.0 Clinical Statement RIM

10. Criterion
CDA R2.0 Clinical Statement RIM

11. External Acts
CDA R2.0 Clinical Statement RIM

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

13. 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”

14. Manufactured Product
CDA R2.0 Clinical Statement RIM

15. Manufactured Product
CDA R Clinical Statement

16. Participant
CDA R2.0 Clinical Statement RIM

17. Performer
CDA R2.0 Clinical Statement RIM

18. Participant / Performer
CDA R2.0 Clinical Statement RIM

19. Participant / performer
CDA R2.0 Clinical Statement RIM

20. Specimen
CDA R2.0 Clinical Statement RIM

21. Specimen
CDA R2.0 Clinical Statement RIM

22. Specimen
CDA R2.0 Clinical Statement RIM

23. 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

24. Observation Range & Criterion
Clinical Statement