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, ...

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 ...

The use of deception or incomplete disclosure limits the subject's ability to make a fully informed decision of whether to participate in the research — one of the essential ethical concerns in human ...

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 language used in consent forms for people volunteering to take part in medical experiments is too difficult for most people to understand, a survey has found. Legally and ethically, participants ...

Can a Physician Delegate the Informed Consent Process? Problem With an Informed Consent Prior to Surgery Lawyers Weigh in on Informed Consent The Right Way to Have These Discussions References The ...

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.