The most current versions of HRPO forms are listed and can be downloaded directly to your computer.  Please be sure to download a new copy of the form(s) prior to each submission to the HRPO to ensure the most current form is being used.  Forms are available in both Word (.doc) and Rich Text Format (.rtf).

What forms are you looking for?

• Behavioral Forms
• Biomedical Forms
• Appendix Forms
• Final Report:
  • Word Document (.doc) NEW
  • Rich Text Format Document (.rtf) NEW
• Other Forms

---

Behavioral Forms

Form Title	Word Format	Rich Text Format
Human Research Determination Form	.doc	.rtf
Exempt Study (Behavioral)
Exempt Application REVISED	.doc	.rtf
Information for Participants in Exempt Research	.doc	.rtf
Exempt Protocol Template REVISED	.doc	.rtf
New Expedited Study (Behavioral)
New Expedited Study REVISED	.doc	.rtf
Expedited Protocol Template REVISED	.doc	.rtf
Consent Documents (Behavioral)
Behavioral Consent Template: Is It Right for Your Study?	.doc	.rtf
Consent Template, Number Format	.doc	.rtf
Consent Template, Paragraph Form	.doc	.rtf
Information Sheet: Generic Study	.doc	.rtf
Information Sheet: Psychology Study	.doc	.rtf
Waiver of Consent Documents (Behavioral)
Waiver of Written Documentation of Consent	.doc	.rtf
Waiver or Alteration of Informed Consent	.doc	.rtf
Other Forms (Behavioral)
Modification Request REVISED	.doc	.rtf
REVIEW PROCESS: Modifications received in a given week by Friday at noon will be reviewed on the following Monday. You will receive feedback by email (questions/request for clarification) or an approval within 2-3 days of review.
Continuing Review REVISED	.doc	.rtf
REVIEW PROCESS: Continuations are reviewed in the order they are received. Submit renewal paperwork at least six weeks in advance to ensure enough time for review and clarification of any contingencies.
Final Report Form NEW	.doc	.rtf

Biomedical Forms

Form #	Form Title	Word Format	Rich Text Format
Form 1:	Request for Review of Research Proposal Involving Human Subjects (Greater than Minimal Risk)	.doc	.rtf
Form 22:	Request for Review of a New Exempt Research	.doc	.rtf
Form 23:	Request for Review of a New Expedited Research	.doc	.rtf
Biomedical Consent Documents
Form 2:	Informed Consent for Participation in Research Activities	.doc	.rtf
	Suggested Language: Please note, separate consent forms are needed for minors and adults. When developing a minor consent form, replace the adult signature lines with those designated for minors in the suggested language.	.doc	.rtf
	Approved Foreign Language Short Consent Templates Arabic (.pdf) Bosnian Cyrillic (Russian) (.pdf) German French Italian Kurdish (.pdf) Non-English Template Spanish (Latin American) Vietnamese (.pdf)
Form 4:	Investigational Drug Data Form	.doc	.rtf
Form 5:	Revision or Amendment to an Approved Protocol	.doc	.rtf
Form 7:	Continuing Review Report for Full Board Protocols	.doc	.rtf
Form 7a:	Continuing Review Report for Expedited Categories 1-9 Studies	.doc	.rtf
Form 8:	Multiple Project Proposal	.doc	.rtf
Form 10:	Publication or Presentation of a Clinical Case Study	.doc	.rtf
Form 11:	Single Patient Emergency Treatment Using an Investigational Drug, Device or Procedure	.doc	.rtf
Form 12:	Single Patient, Request to Treat	.doc	.rtf
Form 13:	Single Patient/Emergency Treatment Follow-up Report	.doc	.rtf
Form 16:	Humanitarian Use Device	.doc	.rtf
Form 17:	NCI Central IRB Research (CIRB), Local Facilitated Review	.doc	.rtf
	HIPPA Compliance Form	.doc	.rtf
	Washington University Local Consent Language and HIPAA Authorization/Addendum Form	.doc	.rtf
Form 18:	Advertisement(s) Approval	.doc	.rtf
Form 20:	Research for Data Management/ Analysis Only (Department of Medicine Biostatistics Consulting Center)	.doc	.rtf
Form 22:	New Exempt Research	.doc	.rtf
Form 23:	New Expedited Research	.doc	.rtf
Form 24:	Data/Tissue Repository	.doc	.rtf
Form 25:	Research Involving Prisoners	.doc	.rtf
	Final Report Form NEW	.doc	.rtf

Appendix Forms

Form #	Form Title	Word Format	Rich Text Format
Form A:	Multi-center Research Supported by DHHS	.doc	.rtf
Form B:	Research at Performance Sites other than WUMC, BJH, and SLCH	.doc	.rtf
Form C:	IND/IDE Indications	.doc	.rtf
Form D:	Third Party Consent	.doc	.rtf
Form E:	Minors (0-17 years), Studies Including	.doc	.rtf
Form F:	Pregnant Women, Research Involving	.doc	.rtf
Form G:	HIV Testing	.doc	.rtf
Form H:	Genetic Tissue or Data Collection	.doc	.rtf
Form I:	Audiotapes, Videotapes, and Photograph	.doc	.rtf
Form J:	Sponsored Research	.doc	.rtf
Form K1:	Waiver of Informed Consent	.doc	.rtf
Form K2:	Alteration of the Eight Required Elements of Consent	.doc	.rtf
Form K3:	Waiver of Written Consent	.doc	.rtf
Form K4:	Short Form Written Consent	.doc	.rtf
Form K5:	Partial Waiver of Authorization for Recruitment Purposes	.doc	.rtf
Form K6:	Consent for InVitro Diagnostic Device Studies Using Leftover Human Specimens that are Not Individually Identifiable	.doc	.rtf
Form L:	Cognitively Impaired Subjects, Research Targeting	.doc	.rtf
Form M:	Research Being Conducted Outside the United States	.doc	.rtf
Form N:	Stored Data or Tissue for Future Research, Research Involving	.doc	.rtf
Form O:	Remuneration for Research Involving Washington University Employees	.doc	.rtf
Form P:	Research Related Radiation Exposure	.doc	.rtf
Form Q:	Emergency Department, Research Conducted in	.doc	.rtf
Form S:	Justification for use of a Placebo	.doc	.rtf
Form T:	Financial Conflict of Interest	.doc	.rtf

Other Forms

Form Title	Word Format	Rich Text Format
Request for Copies from HRPO Files	.doc	.rtf