For new projects approved by administrative review, only projects that are using an external IRB are to submit updated documentation of Reviewing (external) IRB approval. Principal Investigators (PIs) ...

Three types of New Projects may be submitted in IRBNet for Administrative Review: requests for human research determinations, reports of emergency use of a test article, and requests to use an ...

Learn whether your research study requires registration on ClinicalTrials.gov, as well as the consequences of not registering a study on the site. Topics relevant to the phase in which researchers are ...

Single IRB Plan: Develop a single IRB plan to provide the name of the reviewing IRB, indicate that all sites have agreed to rely on the proposed single IRB (include letters of support from external ...

All studies conducted through one of the health sciences schools must register each of their studies through the CSR system. Only clinical trials (by NIH definition) conducted through the other ...

If you are conducting research at Boston College in conjunction with another university, hospital, or other institution that has an IRB, you may request an IRB Authorization Agreement (IAA), also ...

Western Michigan University fosters a research environment to promote respect for the rights and welfare of individuals involved in human subject research. Actions of the university will be guided by ...