Please provide your email address to receive an email when new articles are posted on . Informed consent forms for interventional oncology clinical trials are often lengthy and written at too high of ...

A federal regulation called the Common Rule previously requested the public posting of participant consent forms to trials listed in the national clinical study database clinicaltrials.gov, among ...

The Revised Common Rule requires all clinical trials to post an unsigned consent form on a publicly available website. The Revised Common Rule is in effect for studies approved on or after January 21, ...

The U.S. Food & Drug Administration (FDA) issued final guidance (Final Guidance) regarding informed consent titled “Informed Consent: Guidance for Institutional Review Boards, Clinical Investigators, ...

Canadian researchers have published new guidelines intended to make consent forms used in clinical research easier for patients to understand. The guidelines describe 75 core elements for consent ...

(Vienna, August 9, 2022, 10:10 a.m. CEST)— Informed consent forms are overwhelming for patients. They are written at a level that is too high for most patients, thus possibly impeding real informed ...

Why it matters: Informed consent protects participant rights and ensures ethical compliance in clinical research, building trust between patients and investigators. What’s changing: From checklists ...

One size does not fit all: Clinical trial investigator perspectives of disparities in racial/ethnic minority participation in oncology clinical trials. Multilevel factors impacting clinical trial ...