New guidelines emphasize the need for clarity in consent agreements for clinical trials and aim to broaden participation in ...

The goal of the informed consent process is to ensure that the research subject is treated with respect and human dignity. The process does this by safeguarding and advocating for the subject's right ...

SAN DIEGO, CA, UNITED STATES, September 12, 2025 / EINPresswire.com / -- PRP Labs, a national distributor of FDA-cleared regenerative medicine equipment, today announced the release of its Free PRP ...

Potential research subjects must be accurately informed of what a project involves, and given the opportunity to decide of their own free will whether or not to participate. This process may be brief ...

Prior to completing an application, you will need to satisfy training requirements. The Human Subject Research Orientation on Canvas will ultimately save you time in ...

Research by Johns Hopkins epidemiologists has confirmed what some have long suspected about consent forms required of clinical trial volunteers: They use language far too difficult for most people to ...

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 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 ...