
WINTHROP-UNIVERSITY HOSPITAL INSTITUTIONAL REVIEW BOARD (IRB)
IRB Meeting Calendar, Deadline Dates and IRB Membership List
Educational Requirements in Human Subjects Protections
Ethical Codes and Good Clinical Practices
Policies and Guidelines
Federal Agencies
IRB Submission Forms
Frequently Asked Questions
Glossary (in lay terms)
Guidance for Research Participant
Contact IRB
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Guidance for Research Participant
This page has been created to provide you with additional information regarding your participation in research. Winthrop is committed to assuring that all of its research activities involving human subjects are conducted in a way that promotes the rights and welfare of subjects. If you have any complaints, comments, or concerns, Please contact the IRB Administrative Office at:
IRB@winthrop.org
Or by phone at:
(516) 663-2552
In addition, there are many sites that will provide you with additional information regarding participating in clinical trials. The links are provided below:
http://clinicaltrials.gov/info/resources
http://www.fda.gov/oashi/home.html
http://www.hhs.gov/ohrp/outreach (Public Outreach Page)
http://www.winthrop.org/departments/clinical/ctn/about.cfm
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