You're required to have all participants in your study complete an Informed Consent Form. See an example of an Informed Consent Form (pdf). Below are the Bethel University Institutional Review Board’s ...

When dealing with invasive or high-risk procedures (eg, operations, chemotherapy, radiotherapy, immunotherapy), once the treatment decision has been made, the conversation turns to informed consent.

In the coming months and years, clinicians and policymakers in the US should heed the HHS directive to protect the informed consent rights of their patients with intersex variations.

These are tools used by the IRB and are not required to be used/submitted by investigators. Research teams may find them helpful when writing protocols to more clearly understand what the IRB must ...

In the 1920s and 1930s, watches were almost always set at 8:20, which had the aesthetic advantage of being symmetrical and not overshadowing logos but resembled ... All subjects provided written ...

26,27 The study protocol and patient informed consent documentation were approved by the site institutional review boards ... the study was not powered to evaluate these assessments. No formal sample ...

That’s why Planned Parenthood of Southern New England (PPSNE) embraces trauma-informed care, creating an environment where our patients can ... During Pap smears, our clinicians explain every step of ...

The Innovate Project is a four-year pan-UK study funded by the Economic and Social Research Council (ESRC) from 2019-23. Its aim was to explore how children's social care and third sector ...