A treatment consent form that you have new customers fill out before a session at a seitai clinic, esthetic salon, or ...

The goal of the informed consent process is to ensure that the research subject is treated with respect and human dignity. The process does this by safeguarding and advocating for the subject's right ...

Before people participate in research, it is important to provide them with all relevant information. This is important among other things to explain to them what the research involves, what they can ...

This section contains forms and templates that are designed to assist researchers complete the eIRB application process and provide the information necessary for the IRB to conduct a thorough review.

Expedited studies are research projects that meet one of the categories under 46.110 and are detailed in the W&M Procedure for Expedited Review. Full board studies are those the IRB determines does ...

Canadian researchers have published new guidelines intended to make consent forms used in clinical research easier for patients to understand. The guidelines describe 75 core elements for consent ...

Background: Consent forms have become too long and often do little to help people understand the risk elements of their participation in research, instead focusing on risk reduction for research ...

The sample consent forms are being provided to you as a tool. They contain all of the required elements of an acceptable consent form. While we strongly recommend that you follow the format that we ...