Archive: General Page
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MedStar Health Research Institute-Georgetown University Oncology IRB
On January 29, 2002 Georgetown University and MedStar Health, Inc. entered into a Memorandum of Understanding, to organize and operate the MedStar Health Research Institute-Georgetown Universit
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IRB Policies, Guidance, and Manuals
Georgetown University IRB Policies and Procedures IRB Policies and Procedures Manual Submitting to the Georgetown-MedStar IRB System Guidance Where to Upload Documents in Your IRB Applica
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Educational Opportunities, Programs, & Events
OHRP Exploratory Workshops The Office for Human Research Protection announces a new OHRP Exploratory Workshop Initiative. The rapidly changing landscape of biomedical and health-related behavioral
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eRIC (Electronic IRB Submission System)
Click here to be taken to the eRIC submission system The Office of Regulatory Affairs (ORA) and University Information Services (UIS) have initiated a project to implement Click Commerce IRB software
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IRB 101
What is an IRB? IRB is an acronym for Institutional Review Board. The IRB is responsible for the review and approval of all research involving human subjects, as well as scientific validity an
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IRB Updates and New Information (Old Version)
1.18.2017NEW FDA/NIH Requirements for Posting Clinical Trials onto ClinicalTrials.gov: Effective January 18, 2017, according to new FDA and/or NIH requirements, your trial must adhere to the new add
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Institutional Animal Care and Use Committee (IACUC)
The IACUC’s mission is to ensure the proper care and humane treatment of animals.
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Institutional Review Board (IRB)
The Institutional Review Board‘s (IRB) primary role is to safeguard the rights and welfare of all human subjects who participate in research studies conducted by Georgetown.
Category: General Page