The City of Richardson and UT Dallas Partner on New Headquarters for the Richardson Innovation Quarter

The City of Richardson and the University of Texas at Dallas have teamed up on a powerful economic development initiative by partnering on a new Headquarters for the Richardson Innovation Quarter (the IQ HQ). A flyer has been created on this topic. UT Dallas will have a significant presence at The IQ®, where we will …read more

HHS Resources

Office for Human Research Protections (OHRP) Office for Human Research Protections (OHRP) Educational Videos Research Use of Human Biological Specimens and Other Private Information Reviewing and Reporting Unanticipated Problems and Adverse Events Investigator Responsibilities FAQs (OHRP) Research with Children FAQs (OHRP) Prisoner Research FAQs (OHRP) International Compilation of Human Research Standards Compilation of European GDPR …read more

Modifications & Renewals

Modifications All changes to an approved research protocol (including changes to consent forms, recruitment scripts / flyers, study measures, personnel, protocol procedures / activities, etc.) must be reviewed and approved prior to the changes taking effect, except when necessary to eliminate immediate hazards to subjects.  Modifications must be submitted through Cayuse. All changes must be …read more

Glossary

# | A | B | C | D | E | F | G | H | I | J | K | L | M | N | O | P | Q | R | S | T | U | V | W | X | Y | Z # 45 …read more

Principal Investigator Responsibilities

The Principal Investigator The Principal Investigator (PI) is the primary individual responsible for the ethical design and conduct of a research study including the supervision of co-investigators and study personnel. While the PI may delegate tasks to members of their research team, they remain ultimately responsible to ensure all research activities are designed and carried …read more

Post Approval

Once approved, any changes to the protocol (regardless of the scope of the change) may not be implemented by the research team until they have been reviewed and approved by the HSP Office.

Researchers

Obtaining Approval Does this need IRB Review? PI Responsibilities PI Eligibility Levels of Review Items to include in your IRB submission IRB Training Recruitment Informed consent Forms and Checklists Common Mistakes Single IRB After Approval Record Keeping / Data Management Modifications / Renewals Reportable Events Post Monitoring Program Study Expiration / Closure General Guidance HHS …read more

Policies

Institution Policies Institutional Review Board Policies and Procedures Federal Regulations The list below represents a few of the federal agencies from which UTD receives support for human subjects research. The links below reference federal websites or documents that contain policies, explain specific provisions, and provide links to resources for that agency. U.S. Department of Health and …read more

3rd Annual New Faculty Research Symposium

On November 4, 2021, the Office of Research and Innovation hosted the 3rd annual New Faculty Research Symposium. This events provides an opportunity for new faculty members to showcase their research in a “three-minute thesis” style forum, while established faculty consider possible intersections of research interests for collaboration. 

Licensing from UT Dallas

Market the Invention The UTD Office of Technology Commercialization (OTC )uses the online database Inteum to allow industry to search available UT Dallas technologies. We also attend conferences and industry events to promote our technology. Once interests are identified, we will work together with the inventors to describe the technical details and advantages of the …read more

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