1 Scope
2 References
3 Definitions
4 Abbreviations and acronyms
5 Conventions
6 Test suite structure (TSS)
7 Electronic attachment
Annex A – Test purposes (TP)
A.1 TP definition conventions
A.2 Test purposes structure
A.3 Group 1.1: HRN direct sender (XDR) message acquisition and
validation (DSMA)
A.4 Group 1.2: HRN indirect sender (XDM) message acquisition and
validation (ISMA)
A.5 Group 1.3: HRN message Syntactic validation (XSV)
A.6 Group 1.4: HRN message body (PHM report) CDG CDA Conformance
(CCDA)
A.7 Group 1.5: HRN message body (PHM report) CDG CCD conformance
(CCCD)
A.8 Group 1.6: HRN message header (metadata) semantic validation
(mapping with PHM report) (XMSV)
A.9 Group 1.7: HRN adherence monitor validation (AM)
A.10 Group 1.8: HRN ATNA validation (ATNA)
A.11 Group 1.9: HRN document digital signature validation (DSG)
A.12 Group 1.10: HRN patient identification validation (PIX)
A.13 Group 1.11: HRN consent management (CM)
Annex B – Testable item mapping, validation and XML schemas
B.1 Testable item mapping validation between PHMR and metadata
B.2 Testable item syntactic validation by XSD (XML schema language)
file
B.3 Testable item syntactic validation against XML reference
document file
B.4 Testable item syntactic and/or semantic validation by
Schematron 1.5
B.5 Schema for RFC 3881 verification
B.6 Schema for XML advanced electronic signatures (XAdES)
B.7 Schema for XML-signature syntax and processing (Xmldsig)
B.8 Testable item mapping validation between signature document and
metadata
Bibliography