All policies and procedures that pertain to ORSP are housed on this page. Please contact ORSP@broadinstitute.org if you have any questions regarding the policies and procedures listed below.

Policies

Deposition of Genomic Data from Non-Commercial Biospecimen Sources into Open Access Databases

Deposition of Genomic Data from Commercially Available Biospecimens into Open Access Databases

Designating an Institutional Review Board of Record

Addressing Allegations and Findings of IRB Protocol Noncompliance

Evaluating Scientific Validity of Proposed Research Involving Human Subjects

Oversight of Education Regarding Protection of Research Subject Rights and Welfare

Determining When Activities are Overseen by the HRPP

Unauthorized Receipt of Protected Health Information (PHI): Identification, Notification, and Remediation

Eligibility for "Principal Investigator" Status for Institutional Review Board Submissions and Biological Research Registrations

Protection of Human Research Participants

Guidance

Office of Research Subject Protection Auditing of Genomic Sequencing Orders

Human Subjects Research Involving Investigational Devices

Human Subjects Research Supported by the Department of Defense

 

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compliance forms
compliance policies
compliance templates
office of research subject protection

Research Subject Protection