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CONSENT FOR PARTICIPATION IN
RESEARCH
Patients identified for projects that require
personal health data must first sign a written consent form. The form should contain the following: -
·
a summarised explanation of the aims and process of the project ·
benefits to be gained from the project ·
possible negative effects from participation in the project ·
a statement seeking permission which explains that this permission is
voluntary. The form signed by the patient is scanned into
their medical records.
Prepared:
April 1999 Reviewed: February 06, 2009 | |||||||
