Advancing patient protection through proposed Common Rule changes for informed consent

By CenterWatch
Published: November 2017

Research practitioners eagerly anticipated the finalization and publication of the revised U.S. Federal Policy for the Protection of Human Subjects, the Common Rule. This paper discusses the proposed changes, the identification of new elements of informed consent and the effect of the revised requirements on clinical research practice.

To learn more, register for our free white paper Advancing patient protection through proposed Common Rule changes for informed consent.

Please enter in your information below. Fields with an * are required.

Please enter a valid email address to receive an email with a link to download the white paper.   

Please check the types of email communications you would like to receive:

CenterWatch offers a range of white papers for download that investigate and analyze current trends in the clinical trials industry and the impact they have on the research community.

Recent titles from CenterWatch:

eTMF adoption and integration accelerating

Sites smothered by technology solutions

Mobile health picks up momentum