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Stratford IRB Home

Education

CITI

CITI Introduction

Detailed Requirements

Stratford IRB Conferences & Orientation

Upcoming Conferences & Orientation

Prior Stratford IRB Conferences & Orientation

IRB Submission Information & Forms

Submission Information

New Submissions

Full Board Review

Expedited Review

Non Human Subjects Research

Continuing Review

Protocol Deviations & Violations

Unanticipated Problems - Adverse Events

Final Report / Study Closure

IRB Forms & Applications

IRB Board Meeting Schedule and Submission Deadlines

Research Consent Glossary

Protocol Status Definitions

Protocol Status

Approvable with re-review by the chair or his designee

Approvable with re-review by the sub-committee

Approvable with re-review by the full board

Non Human Subjects Research

HIPAA Regulations and Guidance

Submission Information & Forms

The links below provide information and forms specific to the IRB protocol application action required.

IRB Submission Types

IRB Submission Checklist

New Submissions

Continuing Review

Unanticipated Problems / Adverse Events in Human Subjects Research

Final Report / Study Closure

Human Subjects Protection Program (HSPP)

HSPP Conference Materials

IRB Meeting / Deadlines Dates

Updated IRB Forms