Informed consent is one of the primary requirements of research involving human participants. It is important to remember that informed consent is an ongoing process, not a document or single event.

All protocols must detail the informed consent process personnel will use if participants will be involved in the research study. Protocols must use the W&M-approved Informed Consent Form (ICF) linked ...

Click here to watch a short video on what is Exception From Informed Consent research. Acute care research is sometimes conducted under Exception from Informed Consent regulations. In many ...

Using this standard, informed consent remains focused on what information a reasonable person would want to have to make an informed choice about participation; this includes: the nature of the ...

Warning! Sweeping changes in public health are on the rise. The latest word, according to Stat, is that the Department of ...

A key part of the ethical guidelines that govern market research is the concept of informed consent. Put simply, this is the concept that individuals agree to provide data for market research purposes ...

The QuinteT team of researchers pioneer qualitative approaches to optimise recruitment and informed consent to randomised controlled trials (RCTs). To date, the team’s principal innovation is the ...

Study results suggest that “telemedicine represents a unique opportunity to reduce time and travel burdens for patients with cancer considering clinical trials,” according to researchers.

Obtaining informed consent is more than getting a signature on a form. Informed consent is one of the primary ethical considerations underlying research with human subjects. ALL human subject research ...

See the informed consent form template (pdf ... about the subject's rights as a human subject or concerns about the research. I have read (or had read to me) the contents of this consent form and have ...