Category Archives: Compliance

The Emory University Compliance Program Manual 2016

January 11, 2016

Emory’s Office of Compliance and the Internal Audit Division have collaborated to create the Emory University Compliance Program Manual.  Although the Office of Compliance and the Internal Audit Division are separate units with distinct operational charges, both units recognize that a strong compliance program demonstrates the commitment of the University and its employees not only […]

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Controlled Drug Take Back Event

December 1, 2015

The Environmental Health and Safety Office in conjunction with the Emory Office of Compliance and under the supervision of the Georgia Drugs and Narcotics Agency will host a Controlled Drug Take Back Day for drugs used in research.  This event is limited to schedule CI-CV drugs from authorized research users.  The event will take place on December 15, 2015 between the hours of 10am and 2pm at the Whitehead […]

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From The Office of Compliance…Ivan Oransky, MD Presents: Retraction Watch

November 3, 2015

Retraction watch has become famous in the world of academic research for examining the self-correcting nature of science by publicizing the retraction of academic journal articles and digging into the stories behind the retractions.  Dr.  Oransky is co-founder of Retraction Watch and also teaches medical journalism at New York University’s Science Health and Environmental Reporting […]

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Need Assistance With Your Data Management/Sharing Plans? Data Archiving? Compliance With NIH Public Access Policy?

September 30, 2015

Emory libraries provide a number of services to assist researchers in developing proposals.  Emory’s libraries provide access to resources that can aid in pre-award and post-award research administration. Examples of services available include help with data management planning, data archiving, public access compliance, and more. To learn more about how the Emory libraries can help […]

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Office of Research Compliance Calendar of Upcoming Events

April 1, 2015
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Compliance Awareness

February 27, 2015

The Emory University Office of Research Compliance posted to their website guidance regarding obtaining prescription drugs and/or controlled substances for use in animal or bench research.  The guidance addresses frequently asked questions in order to assist Emory researchers with information related to state of Georgia and federal law requirements. Information on controlled substances in research, […]

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Uniform Guidance: New Information Brings Some Good News and More Questions…

January 30, 2015

Uniform Guidance:  New Information Brings Some Good News and More Questions… Over the past month, additional information regarding the implementation of Uniform Guidance has been provided (verbally) by federal representatives at the FDP (Federal Demonstration Partnership) Meeting.  While some information shared was very positive, other information adds complexity to how we will need to administer […]

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National Science Foundation (NSF) Updates the Proposal and Award Policies and Procedures Guides (PAPPG)

January 30, 2015

The National Science Foundation has recently updated their Proposal and Award Policies and Procedures Guide (PAPPG). Many of the changes made in the PAPPG are related to the issuance of the new Uniform Guidance (2 CFR § 200) and references within the Guide have been updated to reflect the new Uniform Guidance rather than the […]

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Office of Research Administration Newsletter’s New Web Address

September 2, 2014

In 2013 the Office of Research Administration Newsletter was transitioned to an online format using one of Emory’s web tools.  This year, we were asked to move our newsletter to a new institutional tool.  This task is complete.  The July/August 2014 edition of Emory’s Research Administration Newsletter is available at:  https://scholarblogs.emory.edu/ranews.  Please update any bookmarks […]

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Process For Review of Confidentiality/ Non-Disclosure Agreements

May 1, 2013

In an effort to improve efficiency and the handling of confidential/non-disclosure agreements (CDAs/NDAs), the OSP Contracts Unit has established a listserv e-mail address to send CDAs requiring review and institutional signature. Effective February 1, 2012, all clinical trial related CDAs/NDAs requiring review and institutional signature should be sent to the listserv e-mail. The listserv e-mail […]

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