HL7 EHR-S FM R2.1.1 - Dental Health Functional Profile, Release 2
2.0.0-ballot - Informative United States of America flag

HL7 EHR-S FM R2.1.1 - Dental Health Functional Profile, Release 2, published by HL7 International / Electronic Health Records. This guide is not an authorized publication; it is the continuous build for version 2.0.0-ballot built by the FHIR (HL7® FHIR® Standard) CI Build. This version is based on the current content of https://github.com/HL7/dhfp-ig/ and changes regularly. See the Directory of published versions

Requirements: CPS.3.5 Support for Research Protocols Relative to Individual Patient Care (Function)

Official URL: http://hl7.org/ehrs/us/dhfpr2/Requirements/DHFPR2-CPS.3.5 Version: 2.0.0-ballot
Standards status: Informative Active as of 2025-12-19 Maturity Level: 1 Computable Name: CPS_3_5_Support_for_Research_Protocols_Relative_to_Individual_Patient_Care

Provide support for the management of patients enrolled in research protocols.

Description I:

The clinician is presented with appropriate protocols for patients participating in research studies, and is supported in the management and tracking of study participants.

Criteria N:
CPS.3.5#01 SHALL

The system SHALL provide the ability to present protocols for patients enrolled in research studies.
CPS.3.5#02 SHALL

The system SHALL provide the ability to capture, maintain and render research study protocols.
CPS.3.5#03 SHOULD

The system SHOULD conform to function AS.9.1 (Support Financial Plan Enrollment), to enable participation in research studies.
CPS.3.5#04 SHOULD

The system SHOULD provide the ability to analyze and maintain patients participating in research studies.
CPS.3.5#05 MAY

The system MAY provide the ability to capture and maintain appropriate details of patient condition and response to treatment as required for patients enrolled in research studies.
CPS.3.5#06 SHALL

The system SHALL conform to function CP.3.3 (Manage Clinical Documents and Notes) to capture patient condition and response to treatment.
CPS.3.5#07 SHOULD

The system SHOULD capture, maintain and render research subject disposition information including date/time and trial phase/cycle of study completion/discontinuation as discrete elements.
CPS.3.5#08 SHOULD

The system SHOULD determine patients eligible for known active clinical research protocols as defined by inclusion and exclusion criteria.
CPS.3.5#09 SHOULD

The system SHOULD present information notifying staff of patient's eligibility for known active clinical research protocols as defined by inclusion and exclusion criteria.
CPS.3.5#10 SHOULD

The system SHOULD capture research protocol deviation information, including any verbatim text of protocol deviation.