Consent Forms and Procedures

Author:

Ervin Ann-Margret,Cobb Pettit Joan B.

Publisher

Springer International Publishing

Reference15 articles.

1. Alzheimer’s Association (2004) Research consent for cognitively impaired adults: recommendations for institutional review boards and investigators. Alzheimer Dis Assoc Disord 18(3):171–175. https://doi.org/10.1097/01.wad.0000137520.23370.56

2. Casagrande SS, Jerome GJ, Dalcin AT, Dickerson FB, Anderson CA, Appel LJ, Charleston J, Crum RM, Young DR, Guallar E, Frick KD, Goldberg RW, Oefinger M, Finkelstein J, Gennusa JV, Fred-Omojole O, Campbell LM, Wang N-Y, Daumit GL (2010) Randomized trial of achieving health lifestyles in psychiatric rehabilitation: the ACHIEVE trial. BMC Psychiatry 10:108. https://doi.org/10.1186/1471-244X-10-108

3. Department of Health and Human Services, Office for Human Research Protections (2008) Engagement of institutions in human subjects research. Available at https://www.hhs.gov/ohrp/regulations-and-policy/guidance/guidance-on-engagement-of-institutions/index.html. Accessed 23 June 2020

4. Department of Health and Human Services, Office for Human Research Protections (n.d.) Protection of Human Subjects 45 CFR §46.116 (a) and (b). Available at https://www.hhs.gov/ohrp/regulations-and-policy/regulations/45-cfr-46/index.html. Accessed 23 June 2020

5. Department of Health and Human Services, US Food and Drug Administration (2014) Informed consent information sheet: guidance for IRBs, clinical investigators, and sponsors. Available at https://www.fda.gov/RegulatoryInformation/Guidances/ucm404975.htm#genrequirments Accessed 23 June 2020

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