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 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 format that we ...

Although exempt research is exempt from some of the federal regulations, in most cases of interaction with participants, a consent process is indicated. It’s important to understand that even though ...

Click here to see (and print if you need to) a copy of the latest form for obtaining "consent, authorization, release and waiver" before interviewing minors. We'll be placing it on the Wiki too.

The European Union’s General Data Protection Regulation requires every organization that collects sensitive personal data from those residing in the EU to ask for clear and specific consent before ...

Most men, other than medical professionals, don’t know what a pelvic exam is. In a nutshell, it’s a procedure that doctors perform on patients to evaluate the patient’s reproductive organs. The exam ...

GINA is a federal law that prohibits discrimination in health coverage and employment based on genetic information. GINA defines genetic information as information about: An individual's genetic tests ...

The three sample GDPR texts will provide a customizable framework for your organization to use and stay compliant. Constantly Updated — The download contains the latest and most accurate details.