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FICE OF HUMAN SUBJECTS RESEARCH, 115 Ramsay Hall Phone: 334-844-5966 e-mail: hsubjec auburn.edu Web Address: http://www.auburn.edu/research/vpr/ohs/index.htm Complete this form using Adobe Acrobat Writer (versions 5.0 and greater). Hand written forms will not be accepted. 1. Protocol Number: 2. Original IRB Approval Dates: From: To: 3. Requested ONE YEAR MAXIMUM Renewal Period: From: To: 4. PROJECT TITLE:.

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An IRB protocol is a group of documents that conveys all the necessary information about your research with human subjects to IRB reviewers (e.g., consent form, IRB application).

All projects that meet the definition of research with human subjects (45 CFR 46.102 ) must be reviewed and approved by an IRB, or receive an exempt determination, prior to beginning the research.

Amendment Form Select the type of Amendment. The choices are Amendment, Continuing Review, or Amendment. ... Select the types of modifications that you are requesting for your protocol. ... Provide a brief description of any changes you are requesting for your protocol. Click Save and RASS will unlock your protocol for editing.

Investigators are responsible for providing the IRB with sufficient information and related materials about the research (e.g., grant applications, research protocols, sample consent documents) so that the IRB can fulfill its regulatory obligations, including making the required determinations under 45 CFR 46.111 and, ...

Protocols approved by the IRB, whether under expedited or full board review, are required to undergo continuing review at least annually on or before the expiration date set at the time of approval for as long as recruitment and data collection is to take place, and/or private identifiable data is kept.

IRB Submission Checklist Application. Consent Document(s) Recruitment Materials. Study Instrument(s) Permission Letters (if applicable) Certificate of Education (if not already on file) Grant proposal narrative (if applicable) The application materials have been made into one PDF.

To prepare for a submission to the IRB, the investigator must generally develop a protocol (not required for studies that meet the criteria for exemption), any relevant consent form(s), recruitment materials (written or printed in alternative media, as applicable), and complete the IRB's electronic application in eIRB.

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© Copyright 1997-2025
airSlate Legal Forms, Inc.
3720 Flowood Dr, Flowood, Mississippi 39232
Form Packages
Adoption
Bankruptcy
Contractors
Divorce
Home Sales
Employment
Identity Theft
Incorporation
Landlord Tenant
Living Trust
Name Change
Personal Planning
Small Business
Wills & Estates
Packages A-Z
Form Categories
Affidavits
Bankruptcy
Bill of Sale
Corporate - LLC
Divorce
Employment
Identity Theft
Internet Technology
Landlord Tenant
Living Wills
Name Change
Power of Attorney
Real Estate
Small Estates
Wills
All Forms
Forms A-Z
Form Library
Customer Service
Terms of Service
DMCA Policy
About Us
Blog
Affiliates
Contact Us
Privacy Notice
Delete My Account
Site Map
All Forms
Search all Forms
Industries
Forms in Spanish
Localized Forms
Legal Guides
Real Estate Handbook
All Guides
Prepared for You
Notarize
Incorporation services
Our Customers
For Consumers
For Small Business
For Attorneys
Our Sites
US Legal Forms
USLegal
FormsPass
pdfFiller
signNow
airSlate workflows
DocHub
Instapage
Social Media
Call us now toll free:
1-877-389-0141
As seen in:
  • USA Today logo picture
  • CBC News logo picture
  • LA Times logo picture
  • The Washington Post logo picture
  • AP logo picture
  • Forbes logo picture
© Copyright 1997-2025
airSlate Legal Forms, Inc.
3720 Flowood Dr, Flowood, Mississippi 39232