Standardized Text for IRB-01 Informed Consent Forms

 

Form Last Update
Blood draw risk 04/24/2007
Certificates of Confidentiality 11/29/2017
Clinicaltrials.gov language  05/15/2012
Employee subjects 02/13/2012
GINA 10/26/2011
GWAS consent addendum 08/16/2013
Internet Search Language 03/04/2015
LAR Addendum: Risk for Loss of Capacity 03/18/2016
Magnetic resonance imaging 04/24/2007
Placebo/Randomization 04/24/2007
Phase I study benefit language (Question 11.a.) 05/22/2012
Question 14. If you choose to take part in this study, will it cost you anything? 12/21/2016
Question 15. Will you be paid for taking part in this study? 01/31/2017
Question 16. What if you are injured because of the study? 10/31/2017
Radiation 06/06/2008
Reading Exception Language (put in Question 7 of the Informed Consent). 09/10/2010
Reproductive Risks (pregnancy) 06/20/2008
Storage of Tissue 05/17/2013
Student Subjects 04/24/2007
 Suicidal – Surveys/Questionnaires eliciting Suicidal Information 02/18/2016
Recording Subjects: photographs, video recordings, and/or audio recordings 04/04/2013
You/Your Child box templates 05/15/2012
VA EFT Compensation 06/18/2014
“Waiver of Documentation of Informed Consent” Sample Letter 04/04/2013