Archive: General Page

  • ORQA Training & Education

    Clinical Research Coordinator Seminar Series 2023 Monthly Meeting Schedule and Information Previous Recordings and Handouts CRC Essential Training Materials Billing Compliance and OnCo

    Category: General Page

  • ORQA Study Tools & Templates

    Study Tools ALCOA-C ChecklistConsideration for Re-consentingCRC Hand-Off Checklist for CRC Handing-Off StudiesCRC Hand-off Checklist for CRC Receiving StudiesWeekly Team Meeting ChecklistInternal

    Category: General Page

  • Georgetown University DSMC

    About The Data and Safety Monitoring Committee (DSMC) is an independent group of experts housed within Georgetown University. The members of the DSMC are tasked with the responsibility of prospect

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  • Clinical Research Policies and SOPs

    Joint GU/MHRI Policies and Procedures Policy MG.O-001 — Clinical Research Billing Compliance with Medicare Requirements (Version Date: 12/01/2021) Procedure MG.O-001.01 — OnCore Pathway to Bill

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  • ORQA Policies and Resources

    Clinical Research Policies/SOPs Study Tools & Templates COVID-19 Resources

    Category: General Page

  • Export Controls and International Research Collaborations

    This webpage is intended to provide you with information on the export control regulations affecting research at Georgetown. This section contains links to the internal Georgetown University policies

    Category: General Page

  • Overview of Export Control Regulations

    Export Administration Regulations (EAR) The Export Administration Regulations, issued by the U.S. Department of Commerce and located in 15 CFR §§ 730-774, govern “dual use” technologies and produc

    Category: General Page

  • Georgetown University Research and Export Controls

    Fundamental Research Exclusion Much of the research that is conducted on the Georgetown University campus qualifies for the fundamental research exclusion to the export control laws. Fundamen

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  • International Research Relationships and Activities

    The Bureau of Industry and Security (BIS) amended the Export Administration Regulations (EAR) by adding 37 entities to the Restricted Entity List. The Entity List identifies entities for which there is reasonable cause to believe, based on specific and articulable facts, that the entities have been involved, are involved, or pose a significant risk of being or becoming involved in activities contrary to the national security or foreign policy interests of the United States.

    Categories: Export and Sanctions Updates, General Page

  • Meeting Deadlines & Dates

    For details including a combined calendar of meeting deadlines and dates for all five IRB committees as well as separate tables for each Committee’s meeting deadlines, dates, locations, and tim

    Category: General Page