What's New Archived 2005

12/19/05

• IRB Board 1 Roster Updated

11/28/05

• The Board 2 meeting scheduled for December 19, 2005 has been cancelled due to lack of quorum.

11/19/05

• Submission Process Updated - Link to Human Biological Specimens Guidance
• IRB Board 1, 3, 4 Rosters Updated
• IRB Board 5 Roster Added

11/18/05

• Revised IRB Form - Human Cell Lines and Derived Products
• IRB Contacts Updated
• Submission Process Updated - Link to SRC Policy Regarding Tissue Studies

10/17/05

• Revised IRB Form - Human Cell Lines and Derived Products
• Revised HIPAA Form - Research Privacy Form 4 PHI Research Authorization

10/14/05

• 2006 Board Meeting Schedules

09/15/05

• New IRB Form - Human Cell Lines and Derived Products

09/02/05

• IRB Policy (Consent Documentation) 701, Section 1.3.B.1: The requirement for a certified/notarized attestation by a translator has been revised to just a written attestation from the translator.
• Clarification added on the use of the short form.

08/30/05

• Federalwide Assurance Affiliate List Updated

08/29/05

• IRB Board 4 Roster Updated

08/11/05

• Consent Form Template - Signature section revised.
• Consent for Non-English Speaking Subjects

07/28/05

• IRB Application (pdf) has been updated to reflect HRPP requirement questions for PI, Co-PI, Sub-I's and Coordinators.  Please download the most recent version of this document (07/28/2005) for use.  Also note that any person listed on a New Application (protocol modification or continuing review) must have completed HRPP requirements as outlined in Education in Human Research.  Submitted documents will be returned until HRPP requirements are satisfied or personnel are removed from the document (and the conduct of the study).

06/30/05

• Forms for reporting Protocol Deviations and Unanticipated Changes

06/24/05

• New IRB Policies & Procedures (effective 7/1/05)

06/14/05

• Adverse Event submission instructions revised

05/31/05

• IRB Board 1, 2, & 3 Rosters Updated
• HIPAA Research Privacy Forms (1-10) - removal of extra version date

05/19/05

• Be prepared!!  Updated information related to purchasing an Adobe license can be found on the IRB Forms page.  Please note:  In the very near future, all IRB forms will be converted to Adobe .pdf format.  It will be necessary for you to acquire your Adobe license so that you will be able to utilize the .pdf forms.  Word versions will be outdated and no longer accepted.  This conversion will take place over the summer months of 2005.  Get your license today!
• If you have downloaded the .pdf or Word version of the IRB Application for New Research to your hard drive, be advised that you may not have the most recent version.  The latest versions are dated 5/2005.  Please check your saved version and update your hard drive if needed.  If you submit an outdated version of the IRB application, it may be returned to you.  Save yourself some time by checking (NOW) to make sure you have the latest version of the IRB Application.

05/02/05

• IRB Board 1 Roster Updated

02/28/05

• All 4 IRB Board Rosters Updated

02/18/05

• Consent Form Template - New Version To Use
• Consent Form Template - New Version With Yellow Highlights for Change Reference

02/16/05

• Quality Improvement Program
• Federalwide Assurance
• Participant Outreach Program
• Frequently Asked Questions

02/14/05

• IRB Contacts Updated

01/06/05

• HIPAA Research Privacy Forms (1-4)
  Removal of Privacy Office email address

01/03/05

• Submission Deadlines and Number of Copies