Central IRB Research (CIRB)

For more information about the CIRB initiative, please visit the CIRB website: http://www.ncicirb.org/

All events following the initial review such as renewals, revision/amendments, data monitoring progress reports should be submitted to the PRMC and the HRPO with the CIRB application form for the event and the applicable revised CIRB approved documents (i.e. protocol, investigator’s brochure, revised CIRB approved consent form including WU standard statements).

Note: Forms on this page are only available in Rich Text Format (.rtf).  For forms in Word format please visit the All Forms page.

Forms

• Form 17: NCI Central IRB Research (CIRB), Local Facilitated Review Revised
• HIPAA Compliance Form
• Washington University Local Consent Language and HIPAA Authorization/Addendum Form

Appendix Forms

• Form B: Research at Performance Sites other than WUMC, BJH, & SLCH Revised
• Form C: IND/IDE Indications Revised
  • Form 4: Investigational Drug Data Form
• Form D: Third Party Consent
• Form P: Research Related Radiation Exposure Revised
• Form Q: Emergency Department, Research Conducted in New
• Form S: Justification for use of a Placebo
• Forms K1-K6: Consent Alternatives
• Form T: Financial Conflict of Interest

Helpful Information

• Confidentiality Classifications
• Department Approvers List
• HIPAA Identifiers
• Standard Interviews/Questionnaires

Last updated: 1/9/09