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 ...

The Bureau of Labor and Industries issued the final rules regarding the changes to the manufacturing overtime laws on December 27, 2017. The rules became effective on January 1, 2018. You can view the ...

Informed consent is an agreement between the investigators and the research participants. A signed informed consent form notifies potential research participants of their obligations and rights, and ...

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 consent forms signed by patients who take part in medical studies are written in such complex language that most Americans could not understand them, a study suggests. The study looked at the ...

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 ...

The Initial Protocol Application, like all of the HRPP webforms, is an interactive form with built-in logic. That means that the answers to some questions will reveal other questions. Only the ...

Care at Your Fingertips: Codesign, Development, and Evaluation of the Oncology Hub App for Remote Symptom Management in Pediatric Oncology We surveyed institutions in the National Comprehensive Cancer ...