The ERC's processes are built on the belief that the work between the researcher and the IRB is a collaborative process.

In spite of the potential risks of a given clinical trial, research participants willingly put their trust in the Principal Investigator and his or her staff.  It is this trust that provides the Investigator with the privilege of conducting research. This trust must be protected through the application of basic ethical principles which include respect for persons, beneficence, and justice.

To achieve this goal of protection, the ERC is committed to working as a partner with the Principal Investigator and their staff to build a solid working relationship based on effective communication, essential not only to educate researchers on regulatory requirements, but also to ensure that the ERC staff understands the practical issues which occur at the research site.

This section is designed to assist the research site with the submission process, ongoing reporting, continuing review, and to assist in easing communication with the ERC.  

If you have additional questions not covered in this section, please contact the ERC administrative office for assistance.