Non-Medical Research Consent Form

INFORMED CONSENT DOCUMENT TEMPLATE: …

https://und.edu/research/resources/human-subjects/_files/docs/informed-consent-template.doc

This consent document template is recommended for non-medical studies because it contains all required elements of consent. ... [The following statement must be included …

Social & Behavioral Research: Forms & Consent Templates

https://researchcompliance.stanford.edu/panels/hs/for-researchers/forms-templates/nonmedical

For questions, please contact the Non-Medical IRB Panel Staff. If you are having trouble accessing these forms, please ask IRB Education ( email or call 650-724-7141) to have …

Consent Templates | UArizona Research, Innovation

https://research.arizona.edu/compliance/human-subjects-protection-program/HSPP-forms/consent-templates

Sample Consent Forms - UNC Research

https://research.unc.edu/human-research-ethics/consent-forms/

Assent Form Ages 15-17. 2020-01-17. Consent Addendum for Unencrypted Communication. 2022-10-21. Information or Fact Sheet. 2020-01-17. The following …

Consent Form Templates | CHOP Research Institute

https://www.research.chop.edu/services/consent-form-templates

Studies have shown that the Flesh-Kincaid can underestimate the difficulty of text related to medical information by 1 - 2 grades. ... Consent Template Exempt Research This …

Informed Consent for Clinical Trials | FDA

https://www.fda.gov/patients/clinical-trials-what-patients-need-know/informed-consent-clinical-trials

Informed consent means that the purpose of the research is explained to them, including what their role would be and how the trial will work. A central part of the informed …

Medical Research: Forms & Consent Templates

https://researchcompliance.stanford.edu/panels/hs/for-researchers/forms-templates/medical

If you have questions or are having trouble accessing these forms, please contact IRB Education ( email or call 650-724-7141). The consent/assent form should be in a …

Informed Consent of Subjects Who Do Not Speak …

https://www.hhs.gov/ohrp/regulations-and-policy/guidance/obtaining-and-documenting-infomed-consent-non-english-speakers/index.html

Subjects who do not speak English should be presented with a consent document written in a language understandable to them. OPRR strongly encourages the use of this …

Obtaining and Documenting Informed Consent of …

https://www.hopkinsmedicine.org/institutional_review_board/guidelines_policies/guidelines/nonenglish_consent.html

January 2021. What are requirements for including non-English speakers in a study? As required by The Department of Health and Human Services (DHHS) regulations (45 CFR …

Ethics Committees - Wits University

http://oceania.generic-mapping-tools.org/srtm3/N45W103.SRTMGL3.jp2

Ethics Committees. Animal Research Ethics Committee (AREC) Biobanks Ethics Committee. Clinical Drug Trials. Human Research Ethics Committee (Medical) Human …