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Please go to www.ahrq.gov for current information.
Privacy and confidentiality are central
- Participants:
- are allowed the use of the data for designated purpose of treatment and diagnosis only.
- signed a Registration Agreement that designates them as a Data Provider and/or a Data Recipient.
- signed a Data Sharing Agreement.
- have a vote on the policy committee known as the Operations Committee
- Patients :
- are notified that their clinical data could be shared with the MidSouth eHealth Alliance..
- have the right to "Opt Out" of the system. It is assumed they are in the system until they "Opt Out".
Documents: http://www.volunteer-ehealth.org
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