Patient Consent

A written or verbal agreement by a health care consumer grantor or a personal representative, made to an authorized entity grantee concerning authorized or restricted actions with any limitations on purpose of use, and handling instructions to which the authorized entity must comply:

- Privacy Consent Directive: Agreement, Restriction or Prohibition to collect, access, use or disclose (share) information.
- Medical Treatment Consent Directive: Consent to undergo a specific treatment (or record of refusal to consent).
- Research Consent Directive: Consent to participate in research protocol and information sharing required.

Attributes

AttributeTypeMultiplicityAttribute note

Relationships

From class From multiplicity Relationship To class To multiplicity
Patient Consent 1 constrained by Patient Consent Provision Event 0..*
Patient Consent 0..* is Document Reference 0..*
Patient Consent 1 covers Privacy Policy 0..*
Patient Consent 0..* managed by Party Role 0..*
Patient 1 subject of Patient Consent 0..*
Provenance 0..1 Patient Consent 0..*
Patient Consent 0..* sourced from Patient Consent 0..*
Patient Consent Role 0..* related to Patient Consent 0..*
Patient Consent 0..* has (aggregation) Attachment 0..*
Patient Consent 0..* scopes Clinical Document 0..*

Contact us

If you have questions about this initiative, would like to be added to our stakeholder notification list or would like to participate in our consultations, please email us.

connectedcare@cihi.ca

How to cite:

Canadian Institute for Health Information. Patient Consent. Accessed November 02, 2026.