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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 ...

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 ...

Note to researchers: Protocols submitted after 4 PM on Fridays (or the last business day of the week) will be reviewed the following week by the IRB Analysts. The IRB Analysts make efforts to review ...

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 ...

As with Boston College's Jesuit tradition of excellence, service and beneficence, the goal of the IRB is to ensure the safe and ethical treatment of research participants. The University ethics ...

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 ...

Iqure Pharma Inc. has received institutional review board (IRB) approval for a first-in-human study of iQ-007 in healthy volunteers. This follows recent formal approval from the Human Research Ethics ...

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 ...