研究与监管事务办公室 (IRB)
...到 review and 在spect 这 ethical conduct of human participant research, adherence to the study protocol, and adherence 到 what is presented to the IRB as well as 到 participants in the informed consent process. Audits typically 在volve 这 review and 在spection of 在formed consent 为了ms, HIPAA authorization 为了ms, IRB records, training documentation and data management/documentation with an emphasis on...