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 ...

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 ...

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 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 ...

Informed consent is one of the most important aspects of conducting ethical research with human participants. Respecting the autonomy of research participants, the investigator must provide complete ...

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, ...

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.

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.

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 ...