Informed consent is more than just a form; it is a process that actively involves the participant. It is an "ongoing exchange of information between the investigator and [participant]" per the OHRP.

Institutional review boards (IRBs) are charged with safeguarding potential research subjects with limited literacy but may have an inadvertent role in promulgating unreadable consent forms. We ...

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 ...

Informed consent is one of the primary requirements of research involving human participants. It is important to remember that informed consent is an ongoing process, not a document or single event.

Ever wonder what happened to the case of the “exotic dancers” who claimed that they were misclassified as independent contractors? Well, the case continues and yesterday, the federal court denied a ...

Allow Student Health Services to provide health care to a student who is under 18 years of age. This form must be completed if the student is under 18 years of age when they arrive on campus or at the ...

Health data’s potential can be vertigo-inducing, with seemingly limitless insights available to be mined from data sets old and new. The risks, too, can turn the stomach: faulty and biased algorithms; ...

L O S   A N G E L E S, Jan. 7 -- The practice of having prospective sex partners sign consent forms before things heat up may be a sign of the times. Ava Cadell, a Los Angeles-area sex therapist, ...

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.