For research involving UAB students or employees, the appropriate statement must be included (see Sample Informed Consent Document ). Disclosures. In seeking informed consent, the following ...

Several sections under General Information contain guidance about consent and assent: IRB-Review—Outcomes-and-Approval-Details; Conducting the Protocol; Participant Populations; The UAB IRB also ...

The Informed Consent Form should be in the primary language of the research participant, or at least in a language in which the participant is considered fluent. The investigator should submit a ...

Even a patient-signed informed consent document won't necessarily hold up in court, because informed consent is not simply a form; it's a process. At Stanford University Medical Center, ...

The informed consent portions of the training involved reading the relevant law and sample documentation for clinical drugs trials and psychology experiments involving children.

Researchers are expected to use simple non-scientific terms in the informed consent forms. But because stem cell research is such a complex topic, it may be difficult for patients to understand ...

The consent process for phase I studies is always challenging because of divergent perspectives on the prospect of benefit in a phase I trial. 3,4 In addition, the stress and variable cognitive ...