This title is part of a longer publication history. The full run of this journal will be searched. TITLE HISTORY A title history is the publication history of a journal and includes a listing of the ...

using infectious agents with research participants the IBC protocol involves the use of human research participants or identifiable human biospecimens An IRB protocol submission is not required to the ...

If the circumstances necessitate modifying a conflict mitigation or management plan, you should reach out to the Office of the Vice President for Ethics and Compliance (or IRB for research-related ...

that prevents you from submitting your form, please reach out to [email protected]. ROAMWyo Human Ethics (IRB) - Video 1 - Submitting a New Study ROAMWyo Human Ethics (IRB) - Video 2 - Additional ...

Univo IRB has announced the launch of its Canadian research ethics board (REB) review services, aimed at supporting clinical ...

Federalwide Assurance (FWA) and Institutional Review Board (IRB) assurances with OHRP/FDA have been obtained for both SFU and the SFU Research Ethics Board (REBs in Canada are referred to as IRBs in ...

Researchers across many disciplines are increasingly utilizing artificial intelligence (AI), including large language models (LLMs) such as ChatGPT to support empirical research and data analysis, ...

The IRB is authorized to approve, require modifications in (to secure approval), or disapprove all research activities using human subjects covered by this policy. Qualifying research can be ...