Adverse Event Clinical Research
1.0.1 - STU1 International flag

Adverse Event Clinical Research, published by HL7 International / Biomedical Research and Regulation. This guide is not an authorized publication; it is the continuous build for version 1.0.1 built by the FHIR (HL7® FHIR® Standard) CI Build. This version is based on the current content of https://github.com/HL7/fhir-ae-research-ig/ and changes regularly. See the Directory of published versions

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Page standards status: Informative

Provenance for Observation/weight-janet

Summary

Recorded2023-04-12 15:26:23+0000

Agents

Typewho
Author: Provenance Author. Will be reference to the PractitionerRole that authored the measurement. Needs to include a reference to the organization that is responsible for the measurement, at a minimum
InformantPatient/JanetPatient: Janet, the patient who informed the system of the weight authored by the ProvanceAuthor " CLINICAL TRIAL PATIENT"