How do I begin?
Guide to Developing a Protocol
Chart Reviews
Barcode... download barcode font for letters...
(right click on this link, select save target as, save this file to c:\windows\fonts).
If you have problems please contact your Lan Administrator or the DIS Helpdesk.
Database Authorization
Convened Review
FWA letter Federal Wide Assurance Number is 00003630. Expires 9/29/08.
Forms
Guidelines for Recruitment Materials
Guidelines for Investigators that plan to use Clinical Laboratory Services personnel. Requests to the Clinical Laboratory such as for patient phlebotomy, specimen processing, specimen shipping, and/or laboratory analyses by University Hospital & Clinic employees for clinical research studies must adhere to the following policy and procedures: read more...
Investigator Responsibilites
IRB "Process"... what happens to your protocol after submission
IRB Review Fees
Lay terminology
Legally Authorized Representatives - who may give consent for another
Patients and Research...who may approach to seek their participation?
Policies & Procedure Manual
Policy on IRB Rosters
Registering a Clinical Study in a Public Registry
Tracking Changes in a Word document
10 Things to Speed up IRB Review Time The IRB has identified the most common omissions and deficiencies in submissions. Attention to these details “up front” should speed the review of your protocols. Please feel free to contact the IRB office for assistance or for “pre-review” of your submission documents.
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