Academic research involving human subjects — from a straightforward interview to advanced biomedical testing — raises a host of difficult technical and ethical questions. To ensure that students and ...

A series of reforms is underway that the University hopes will streamline Institutional Review Board procedures involving the ethical treatment of human research subjects. In response to ...

HOUSTON, TX, Feb. 18, 2025 (GLOBE NEWSWIRE) -- Nexalin Technology, Inc. (Nasdaq: NXL; NXLIW) (the “Company” or “Nexalin”) the leader in Deep Intracranial Frequency Stimulation (DIFS™) of the brain, ...

The University IRB has the authority to suspend or terminate IRB approval of research that is not being conducted in accordance with IRB requirements or that may pose unexpected, serious harm to ...

Research with human participants in countries outside the United States must comply ethical standards. Additional considerations may be required depending on the country of research. Furthermore, ...

Investigators must use Cayuse to electronically submit new research studies for review and approval, course approvals, continuing research requests, amendments to approved research studies, and ...

The IRB reviews research involving human subjects if one or more of the following apply: The research is sponsored by WMU, regardless of the location of the project. The research is conducted by, or ...

Informed consent is one of the most important aspects of conducting ethical research with human participants. Respecting the autonomy of research participants, the investigator must provide complete ...

Obtains information or biospecimens through intervention or interaction with the individual, and uses, studies, or analyzes the information or biospecimens; or Obtains, uses, studies, analyzes, or ...

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 ...