Riley Rosenquist
Biography
The Regulatory Affairs (RA) team provides regulatory oversight and management of all ATRI and ACTC trials and ensures that all research activities are in compliance with HHS regulations related to the protection of human research subjects. RA’s activities include consent form development, site essential document and Trial Master File (TMF) management, central IRB submissions, and general Good Clinical Practice compliance across ACTC and ATRI.
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