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 short form written consent process does not apply when: research is exempt, including IRB-Flex exempt ... item (c); or the investigators expect the sample population to include participants who do ...

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 ...

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 ...

Neither the level of research funding received from ... Downstate Medical School have presented informed-consent templates and sample forms that are below an 8th-grade reading level.

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, ...

The sample consisted of 246 consent forms ... Description of the Purpose and Procedures of the Research The consent forms were also assessed for a description of the trial as research, mention ...

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