Obtaining informed consent is more than getting a signature on a form. Informed consent is one of the primary ethical considerations underlying research with human subjects. ALL human subject research ...

using language appropriate to your specific research, setting, and participants. There is no need to utilize the UAB IRB’s Sample Consent form for consent processes in exempt research. Your consent ...

a model consent form included in the protocol and listed in the Table of Contents of the protocol with the same wording, or in the contract or agreement. An explanation of whom to contact for answers ...

and agree or decline their child’s participation in the research study. Investigators should follow the required elements of informed consent when preparing a Parental Consent Form, except that the ...

A waiver of the need for subjects to sign a consent form can be granted if any one of the following three conditions are met: The only record linking the subject and the research would be the consent ...

Give the contact information of the Brandeis University HRPP (hrpp@brandeis.edu or 781-736-8133) for questions about the subject's rights as a human subject or concerns about the research. I have read ...

A free-form research plan is not accepted ... Are there ethical issues (e.g. ethical governance procedures, informed consent, and anonymity of subjects) that need to be taken into account when ...

Use a signed consent form to record this consent ... their knowledge of the person with dementia to help staff to do this. When is it appropriate to research the experience of people with dementia who ...

The information and sample documents in the compliance form section are provided to help researchers develop consent and assent documents customized to the design of the individual research project.