(1) A data registry to receive and store the data described in this section from coordinated care organizations, health care providers and health insurers, patients, clients and members of coordinated care organizations, health care providers and health insurers, the authority and the Department of Human Services. The registry must allow for coordinated care organizations, health care providers and health insurers to:
(a) Electronically submit data collected under ORS 413.164; and
(b) Query the data registry to determine whether the registry contains current data for a patient, member or client.
(2) Functionality that allows a patient, member or client to directly submit to the data system their data described in this section. [2021 c.549 §2]
Note: See second note under 413.161.