Read this article to learn about online informed consent training for clinical trials, using a collaborative approach.

Recent research is showing medical treatment for pregnant women often relies on clinical data from non-pregnant female ...

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.

consent must be re-requested from the participant, who must re-read lengthy forms containing complex terminology, which can affect retention. It isn’t abnormal for clinical trials to require ...

The primary value of placebo controls in clinical trials is the minimization of bias.

Data in and of itself can be interesting, but the true value of data lies in how you use it and the insights that come from ...

The survey assessed patients' preferences for telemedicine versus in-person visits for the IC process and their comfort with discussing clinical trials virtually. The primary outcome was the ...

The Revised Common Rule includes a requirement specific to clinical trials to post an informed consent form used to enroll participants on a publicly available website. A study involves the ...

You understand the possible benefits and risks of participating in a clinical trial. You have signed and submitted your informed consent form. Before you decide to take part in a clinical trial, ...