Protocols must use the W&M-approved Informed Consent Form (ICF) linked below. Consent documents should be maintained by the PI for at least 3 years beyond the end of the study. Information about ...

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 consent form is one part of the dialogue that investigators have with each subject. It is recommended that forms for adult subjects be written at a 6 th-grade reading level or lower, information ...

If a parent or guardian is not present, you can give them a hardcopy of the consent form to fill out. You can then upload the completed document to your student health portal or send it directly to ...

Part of the document giving consent to inspect a German real estate agent’s luggage had been forged, her defence lawyer told the court on Friday, accusing police of attempting to prove she understood ...

We are working with Guy’s and St. Thomas’ NHS Foundation Trust to produce national standardised SACT regimen-specific consent forms. We want to support clinicians in ensuring all patients are fully ...

Submission documents include: The completed Application Form. Appendices that can include recruitment flyers, consent forms, survey questions, interview questions, personnel form, etc. The submission ...

No protocol, informed consent process, or informed consent document may be modified without prior approval from the IRB unless it is necessary to eliminate an apparent and immediate hazard to one or ...