WebJan 5, 2024 · Use of Approved, Standard Short Forms. January 5, 2024 Lisa Rigtrup. In October 2024, the University of Utah IRB approved a policy change which allowed the IRB to grant general approval of a standard short form document. This change was intended to streamline the procedure for approval of short form documents and relieve administrative … WebSupplemental Forms. Device Form: Used for any study involving medical devices (as defined by the FDA) Specimen Form: Used for any study collecting or using Human biological specimens for research (e.g., organ tissue, plasma, urine, feces, cells). This may include specimens collected as part of routine care for use as part of the research.
Short Form Consent Documents - University of Pittsburgh
WebThe short form consent form is a document, translated into the subject's preferred language, that contains a description of the required elements of informed consent and notes that … WebConsent Short forms for Non-English Speaking Subjects. Copy Request Form. DSMB Charter Template. ... UVA Institutional Review Board for Health Sciences Research Box 800483, Charlottesville, VA 22908. Physical Address: UVA IRB-HSR One Morton Drive, Suite 400, Box 5 Charlottesville, VA 22903. rb0773.shapp.ch
Consent Templates and Resources - Lurie Children
WebShort Form Consent Documents are “generic” research consent forms that have been translated into multiple common languages and are limited to the basic elements of consent. When no IRB-approved study consent form is currently available in a participant’s language, the use of a written Short Form consent, along with an oral presentation of … WebThe IRB has approved the English version of the Short Form; and it was used as the template for the translated versions on the HSO website. Therefore, investigators should use the English version as a template when having the Short … WebThe IRB provides short consent document translations in several commonly understood languages. This abbreviated translation or “short form” (which attests that the elements of consent have been presented orally) may be used to document informed consent in writing for individuals who do not speak English in limited situations. rb0134101b1s1