It’s important to understand that even though consent may not be documented with a signature, as is the case with much of exempt research, consent is still being obtained. For example, when a consent ...

For example, the informed consent for a research study might advise patients in the following way: Over the course of this trial, routine healthcare information, such as [name of test] results and ...

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, ...

Sample IRB Forms. The sample consent forms are being provided to you as a tool. They contain all of the required elements of an acceptable consent form. While we strongly recommend that you follow the ...

A qualitative exploration of the informed consent process in hematopoietic cell transplantation clinical research and opportunities for improvement. Bone Marrow Transplant 52 , 292–298 (2017 ...

A Data Use Agreement (DUA) is a legally binding agreement between the University of Nevada, Reno (University) and an external entity (e.g., another academic institution, private company, federal or ...