Consent
Consent: The Process
Ethical Issues with Informed Consent [PDF]
Informed Consent 101[PDF]
Consent Form Language Tools
PlainLanguage.gov
Plain Language Thesaurus [PDF]
Glossary of medical words in lay terminology [PDF]
Unit Metric Equivalent US Equivalent [PDF]
Common acronyms [PDF]
Other Information About Consent
If your research study includes genetic testing of research subjects, the following statement can be added to the RISKS section of the consent document (after the genetic testing risks):
"There is a Federal law called the Genetic Information Nondiscrimination Act (GINA). In general, this law makes it illegal for health insurance companies, group health plans, and most large employers to discriminate against you based on your genetic information. However, it does not protect you against discrimination by companies that sell life insurance, disability insurance, or long-term care insurance."
HRP-090 - SOP - Informed Consent Process for Research [DOC]
HRP-091 - SOP - Written Documentation of Consent [DOC]
MI-6 2C - Phone Consents for Minimal Risk Research [DOC]
Program for the Protection of Human Subjects
Tel: 212-824-8200
Fax: 212-876-6789
For submissions and general inquiries send e-mail to: IRB@mssm.edu
PPHS Location
345 East 102 Street
(between 1st and 2nd Avenues)
Suite 200
New York, NY 10029
Mailing Address
Icahn School of Medicine
One Gustave L. Levy Place
Box 1081
New York, NY 10029-65749

