The Human Research Protection Program’s (HRPP) primary mission is to protect the rights, welfare and privacy of all individuals participating in research sponsored by the Medical College of Wisconsin and Froedtert Hospital. The HRPP oversees and supports the MCW/FH Institutional Review Boards (IRBs) which review all research studies involving human subjects for safety, compliance with regulations, scientific quality, and ethical standards. The HRPP provides guidance and resources for the MCW/FH IRBs, investigators, and study team members. Ongoing training for researchers and quality improvement activities are directed toward compliance with regulations and scientific integrity.
MCW/FH IRB #2 Meeting 11am MFRC 3075
MCW/FH IRB #3 Meeting 4pm MFRC 3075
Adobe Consent Training 1pm MEB2050
MCW/FH IRB #4 Meeting 12pm MFRC 3075
In a letter dated October 23rd, 2009, The Food and Drug Administration (FDA)/Department of Health and Human Services (DHHS) approved the Centers for Disease Control (CDC) request for an Emergency Use Authorization for the unapproved drug peramivir IV for the treatment of H1N1 virus 2009.
The Consent Builder program for new studies was disabled on October 1. Consent forms for all new studies must use the Adobe of Word-based templates.
Effective September 1, 2009, MCW HRPP office has rolled out an update for NCI Cooperative Group Studies.
*MCW network access required
Committee Meeting Schedules & Membership Lists Committee Members Resources
* MCW network access required