Institutional Review Office

Administrative support for the FHCRC Institutional Review Board (IRB) and Institutional Animal Care and Use Committee (IACUC).

IRO web updates by email: If you would like email notice of substantive updates to the IRO's web pages, click here to send us a request.

 

 

WHAT'S NEW:

Institutional Review Office publishes minimum accepted standards for IRB submissions

As noted in our Summer Newsletter - effective August 1, 2014 the Institutional Review Office will be returning incomplete submissions to the research team.  A list of minimum accepted standards for all IRB submissions can be found here - IRB Submissions - Minimum Accepted Standards.  

 ~IRB Committee D Starts August 1, 2014~ 

The Center's Human Research Protection Program continues to grow.  To keep up with an increasing number of human research projects a 4th IRB has been added.  Committee D will be meeting on the 1st Wednesday of each month.  Our IRB system now includes 4 IRBs with a convened meeting each week.  An updated meeting schedule with agenda deadlines is on the IRB Meeting Schedule page.

~Updated Review Requirements for Multi-Center projects!~ 

In response to new regulatory guidance the FHCRC IRB has updated its requirements for review multi-center research projects.  Some current processes have been eliminated and a few new requirements added.  New Application, Modification, Continuation Review, and Multi-Center Supplement forms have been updated effective May 15, 2014. to reflect the new requirements.  Older versions of these forms will be accepted in the Institutional Review Office until end of day June 30, 2014. All IRB forms are available on the Forms Page. More information about the new requirements can be found on the Multi-Center Studies Page.

 

Updates to IRB Policy 2.20 Training.  Clarifications released regarding who is required to complete Good Clinical Practice Training.

The IRB has released an update to Policy 2.20 Training.  Important clarifications were made to the section regarding who is required to complete Good Clinical Practice Training.  More information, and the updated policy can be found on the Training Page.

  

The Institutional Review Office has moved!

The IRO completed its move to the 2nd floor of the Yale Building March 3rd and is now located on the northwest quadrant of the building adjacent to Technology Transfer.

 

Our new mailstop is J2-100.

 

 


Suggestion box: Do you have suggestions for improving the IRO web pages? Email us.  Other questions about our web pages?  Contact Jason Tharpe, web editor.

All IRO eNewsletters


Institutional Review Board (IRB)

[about the IRB]


FORMS AND INSTRUCTIONS

New Applications
Continuation Review
Modification
Consent

More IRB forms...

GUIDELINES, POLICIES, REGULATIONS

Unanticipated problems and noncompliance reporting requirements
Blood draw [pdf]
Closing a study
Data and safety monitoring
Emergency Use of an Investigational Drug or Device
Genetic research [pdf]
Funding
HIPAA
Investigator guidelines
Policies and procedures
Radiation safety
Regulations

MEETINGS & DEADLINES

TRAINING

Institutional Animal Care and Use Committee (IACUC)

[about the IACUC]


FORMS AND INSTRUCTIONS

Annual update
Application for new study
Revision

More IACUC forms...

GUIDELINES, POLICIES, REGULATIONS

Closing a file
Funding
Regulations

More IACUC policies/guidelines...

MEETINGS & DEADLINES

TRAINING

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