Archive: General Page

  • HIPAA Training

    HIPAA training is available through the Collaborative IRB Training Initiative (CITI). The course can be accessed through the "Optional Modules" link once the "Group 1.Biomedical research investigators

    Category: General Page

  • Contact Info

    Institutional Review Board: IRB-A, IRB-B, IRB-C and Oncology E-mail: irboard@georgetown.edu Phone: 202.687.1506 Fax: 202.687.4847 Address: SW104 Med-Dent Building3900 Reservoir Road, N

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  • Protection of Minors Policy

    Protection of Minors in Research Studies Georgetown University has established a Protection of Minors Policy to protect those under 18 years of age who participate in programs and activities, includi

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  • FDA Information Sheet Guidance for IRBs, Clinical Investigators, and Sponsors

    Investigator-Initiated Investigational New Drug (IND) Applications  Information for investigators about submitting Investigational New Drug (IND) applications to FDA 1. Information for investigators a

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  • Federalwide Assurance (FWA) and IORG Number

    Federalwide Assurance (FWA) Verification Letters Georgetown University FWAMedStar Health Research Institute-Georgetown University IORG for all Georgetown University IRB committees IRB Registra

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  • IRB Fees

    Institutional Review of Privately Funded Research on Human SubjectsAdministrative Review of Commercial IRB Approved Research on Human SubjectsIRB Archived File Request INSTITUTIONAL REVIEW

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  • Report Research Compliance Complaint or Concern

    Complaint or Concern About Research Compliance? The Office of Research Oversight (ORO) would like to hear from you.  If you would like to report a problem or raise questions please call us at 20

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  • Human Subject Protection Training

    Certification that one has completed training in human subject protection in research is required of all Georgetown University faculty, investigators, study coordinators and other individuals directly

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  • HIPAA Regulations

    In the research context, HIPAA establishes the conditions under which PHI may be created, obtained, used or disclosed by covered entities for research purposes. As defined by HIPAA, the term “cov

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  • IRB of Record Forms

    OHRP Guidance: Assurance Process HHS human subject protection regulations and policies require that any institution engaged in non-exempt human subjects research conducted or supported by HHS must

    Category: General Page