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 signed informed consent form notifies potential research participants of their obligations and ... vulnerable populations or complex interventions. You may use this sample tempate to get started.

The child's assent is documented with an assent form, a child-friendly document that outlines the essential information about the research. Children who are able to read and write should participate ...

The goal of this requirement is to increase transparency for federally funded clinical trials and simultaneously create a repository of sample consent forms that may be used as a reference for future ...

Investigators should follow the required elements of informed consent when preparing a Parental Consent Form, except that ... benefit to the research subjects, and the child’s age, maturity, status, ...

Keep in mind that obtaining informed consent is a continuous process throughout the research, not simply a one-time event when a subject signs a form. To ensure informed consent, researchers should: ...

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 ...

We are working with Guy’s and St. Thomas’ NHS Foundation Trust to produce national standardised SACT regimen-specific consent forms ... the content in these forms? The programme is being led by a ...

Informed consent is one of the primary requirements of research involving human participants ... provided the conditions described on the waiver form are fulfilled.

See the informed consent form template (pdf) for more help and sample language. 1. Title of the Study 2 ... and their probability as a direct result of participation in the research and/or from breach ...