For multi-site research, generally the prime awardee is considered the responsible party and must ensure compliance with the posting requirement. The informed consent form must be posted on the ...

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 ...

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

Informed consent is one of the primary requirements of research involving human participants ... provided the conditions described on the waiver form are fulfilled.

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, ...

Many types of clinical trials rely upon voluntary participation. Most clinical studies, but not all, test new drugs. Informed consent is the process of learning the key facts about a clinical trial ...

Acute care research is sometimes conducted under Exception from Informed Consent regulations ... The use of a randomized clinical trial such as this is the “gold standard” for determining what works ...

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 ...

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