Standardized Text for Informed Consent Forms

 

Last Update
Blood draw risk 04/24/2007
Certificates of Confidentiality 11/29/2017
Clinicaltrials.gov language  05/15/2012
Genetic Information Nondiscrimination Act (GINA) 11/05/2021
NIH GDS_GWAS consent addendum 02/06/2023
Internet Search Language 03/04/2015
LAR Addendum: Risk for Loss of Capacity 03/18/2016
Magnetic resonance imaging 04/24/2007
NIH DMS Consent Addendum 1/25/2023
Placebo/Randomization 04/24/2007
Phase I study benefit language (Question 11.a.) 05/22/2012
Question 16. If you choose to take part in this study, will it cost you anything? 12/21/2016
Question 17. Will you be paid for taking part in this study? 08/26/2021
 What if you are injured because of the study? 02/06/2024
Radiation 06/06/2008
Reading Exception Language (put in Question 7 of the Informed Consent). 09/10/2010
New template Recording Subjects: photographs, video recordings, and/or audio recordings 09/01/23
Reproductive Risks (pregnancy) 06/20/2008
Storage of Tissue 05/17/2013
Storage of Tissue (sIRB studies) 11/13/2020
Student Subjects 04/24/2007
Study Subject Return to Research Template 05/18/2020
You/Your Child box templates 05/15/2012
VA EFT Compensation 09/21/2018
“Waiver of Documentation of Informed Consent” Sample Letter 04/04/2013