IRB is required to register every three 3 years If there is a change in

Irb is required to register every three 3 years if

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Protections. IRB is required to register every three (3) years. If there is a change in responsible party an updated registration must be submitted within ninety (90) days. If the IRB is discontinued documentation must also be submitted to the Office of Human Research Protections. IRB Organizational Relationships Since the IRB has been tasked with developing a comprehensive plan for data compilations on human subjects in medical studies and creating the policies and procedures for accessing the data within the portal for both patients, medical staff and students, they will be responsible for being educated and highly experienced with federal and state regulations. They will maintain constant open relationships with administrators, researchers, staff and participants. The IRB will have a solid communication policy that will establish the foundation between the Chief Information Officer, Chief Executive Officer, medical staff, medical school, administration staff, information technology staff, data administrators and participating case studies. The Information Technology staff will have a key role in incorporating the HIPAA regulations within the data repositories and the access of these repositories. On going reports of these security measures will be reported to the Chief Information Officer, Chief Executive Officer and IRB on weekly, monthly, quarterly and annual basis, as required.
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DATA SECURITY AND PRIVACY IN BUSINESS 6 References: HHS Office of the Secretary,Office for Civil Rights, and Ocr. “Summary of the HIPAA Privacy Rule.” HHS.gov , US Department of Health and Human Services, 26 July 2013, . American Psychological Association , American Psychological Association, . Babyar, Julie. “The IRB Structure and Medical Research Reform.” Clinical and Translational Medicine , Springer Berlin Heidelberg, 2 Apr. 2018, .
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