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 ...

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

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 ...

Furthermore, unless the consent process has been specifically waived by the IRB, no subjects may be included in research unless the investigator has obtained the legally effective informed consent of ...