Clinical Research Support

Implementation

Below you will find links to policies, systems, and information that you may find useful while planning the implementation of a trial.  For further information or assistance, contact Clinical Research Support.

Patient Recruitment, Consent, Registration and Withdrawal

Informed Consent


Cancer Consortium Policy:

FHCRC/Cancer Consortium Institutional Review Office (IRO) Policy

SCCA Consent Policies:
Contact the Research Implementation Office (RIO) at 206-288-6607
Translator Policy (UW/SCCA/CHRMC/FHCRC IRB) and Forms

Subject Registration


Consortium Studies (UW and FHCRC):
Patient Accrual Tracking System (PATS) 

Participant Withdrawal Procedure


For Clinical Research Division (CRD) studies, the procedure can be found on FYI under "Procedures." To access FYI, you will need to go to the CORE site and use your login password.

Ordering Medical Records

Coordinating Multi-Center Trials

Data and Sample Sharing Agreements — Intellectual Property

  • Technology Transfer (FHCRC)
    Visit Technology Transfer if you are developing inventions with commercial applications. These inventions include new ways of diagnosing and treating cancer and other diseases and new research tools. The Technology Transfer will cover issues such as:
    • Evaluation of Invention Disclosures
    • Patents and Other Intellectual Protections
    • Marketing Technologies
    • Licensing Technologies

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