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, ...

Department of Health and Human Services (DHHS) regulations for the protection of human participants require that informed consent information be presented in language understandable to the participant ...

Obtaining informed consent is more than getting a signature on a form. Informed consent is one of the primary ethical considerations underlying research with human subjects. ALL human subject research ...

It turns out the NSA has a consent form you can fill out to give the agency permission to monitor your overseas phone calls and e-mail. Executive Order 12333 Consent Agreement Signals Intelligence ...

Obtaining valid consent is a fundamental part of providing quality care and a key ethical and legal requirement in medicine. Issues around consent can, however, trip up even the most experienced ...

Background: Consent forms have become too long and often do little to help people understand the risk elements of their participation in research, instead focusing on risk reduction for research ...

This guide was reviewed by a Business News Daily editor to ensure it provides comprehensive and accurate information to aid your buying decision. If you have a medical practice, it’s easy to think ...