Research Integrity and Compliance


The mission of the Office of Research Integrity and Compliance (ORIC) is to assist the Emory Community and the Office of Research Administration (ORA) staff in promoting research compliance with Emory policies and Federal Regulations. ORIC is available for research compliance inquiries and provides training and support as needed. We facilitate the review of research involving human stem cells. We collaborate with ORA offices and researchers in modifying and creating new polices and guidance. We track changes to current regulations to support Emory's research compliance. We oversee the review of our internal ORA research compliance processes, including FDA and Controlled Substance and Dangerous Drug matters, and investigate and support the Research Integrity Officer (RIO) during the review of research misconduct allegations and research noncompliance investigations.

News

ORI Updated interactive videos "The Lab" and "The Research Clinic"

The Office of Research Integrity (ORI) have updated their interactive videos showing different scenarios in where a research misconduct issue may occur. ORI said that "The Lab and The Research Clinic better reflect current standards of appropriate workplace behavior in research settings." Find the videos below.

The Lab
The Research Clinic

Authorship Infographic

Review this infographic to learn who to include in a publication and the responsibilities of being an author.

Access the infographic here

Training to Prevent Research Misconduct

ORIC works closely with our RIO to educate the research community in the prevention of research misconduct. We are available to present at your lab, school or department.

Schedule a Training

Controlled Substances (CS) and Dangerous Drugs (DD) Quality Assurance and Quality Improvement Program

Our program aims to assist researchers at Emory to remain compliant with federal (DEA) and state (GBP/GDNA) requirements when using CS/DD for research. See our flyer or access what you need to prepare for a visit from these offices. Join us every Tuesday at 9:30 am via Zoom at our Q&A sessions to answer any pressing question about the use of CS/DD in research.

QA/QI Resources
Join us every Tuesday at 9:30 am

Highlights

Contact us!

If you've come across any research compliance issues, feel free to contact us and let us know. We're here to assist!

Submit your concern
Contact the team

Georgia Board of Pharmacy and DEA license registration

Register your new or existing licenses with ORIC; update your license after your renewal.

GBP License
DEA License

IND/IDE Submission Help

Contact us for consultations about your IND or IDE submissions to prevent delays.

Devices
Drugs or Biologics

Register to the Webinar Series

Each webinar of the "Managing Controlled Substances & Dangerous Drugs in Research" series last 30 minutes, with a short presentation and questions from the audience. Find the recordings on our Training page.

Register
Recordings