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Annual Event Summary Form
Annual Renewal/Project Modification form
UPDATED
Annual review policy
Approval Timeframes - Service Level Understanding
Approved and Unapproved Devices in Research
Assent Form - Shriners
Assent Form - Standard
Baculovirus Fact Sheet
NEW
Biosafety assignment for lentiviral vectors
NEW
Biosafety Manual
BSL2-Lab Checklist
Certificates of Confidentiality (CoC)
Child Assent
Children in Research
Clinical Investigational Agents Consisting of Recombinant DNA or Infectious Agents
Clinical Research Billing Schedule
Clinical Trials
ClinicalTrials.gov Registration Requirements
Closure, Suspension & Termination of Studies
Collaborations with Non-OHSU Institutions and Investigators
Combined Phase Studies
Committee Charter
Committee Member Reviewer Form
Conflict of Interest in Research
Conflicts of Interest in Human Subjects Research - IRB Policy
Consent and Authorization Forms - Clinical (4.25.2013)
Consent and Authorization Forms - Knight Cancer Institute (5.3.2013)
Consent and Authorization Forms - Non-Clinical (4.25.2013)
Consent and Authorization Forms - Repository Only (4.25.2013)
Consent and Authorization Forms - Shriners (10.30.2012)
Consent and Authorization Forms INSTRUCTIONS (4.25.2013)
Consent Form - Short - Chinese
Consent Form - Short - English
Consent Form - Short - Farsi
Consent Form - Short - German
Consent Form - Short - Instructions for Use
Consent Form - Short - Russian
Consent Form - Short - Serbo-Croatian
Consent Form - Short - Spanish
Consent Form - Short - Vietnamese
Consent Form - Treatment Use of Drug or Device (6.28.2012)
Consent Form Language - Gene Transfer Studies (6.28.2012)
Consent Form Signature Templates - Children Ages 15-17
Continuing Review
Cost Language
Data and Safety Monitoring
Data Use Agreement: Research
Decisionally Impaired Adults in Research
DSMP Template Form
eIRB Hard Copy Submission
eIRB System
eIRB System - Documentation of Approval
Elements of Informed Consent
Emergency Single Time Use of a Test Article (Drug, Biologic, Device)
Engagement in Research
Enrollment Incentives and Finder's Fees
Exempt Review
Expedited Review
Federal Wide Assurance (FWA)
Forms, IRB
Functions and Responsibilities
Genetic Research
HIPAA Authorization for Obtaining Existing Records Outside of OHSU
HIV Information Sheet
Human Subjects Research in the Future
Humanitarian Use Device (HUD)
IBC Questionnaire for Human Subjects Studies
IBC Review of Work with Animals
Updated
Individual Investigator Agreement (IIA)
Infectious Agent/Toxin Questionnaire (IAQ)
UPDATED
Information Sheet Template (2.14.2013)
Informed Consent
Initial Classification Form
UPDATED
Initial Submission Guide
Institutional Reporting Requirements (IRB)
International Research
Investigational Drug Research
IRB Authorization Agreement - OHSU Providing Oversight
IRB Authorization Agreement - OHSU Waiving Oversight
Lab Safety Manual
Lay Language Protocol Summary
Legacy Collaboration - Submission Checklist
Legacy Collaborations - Consent Language
Liability Language - Subject Injury (Updated 7.10.2012)
Member Conflict of Interest policy
Modifications
Obtaining & Documenting Informed Consent From Subjects with Limited English Proficiency
OHSU Students as Subjects
Payments to Research Participants
PI Eligibility Policy
Planned Emergency Research
Prep to Research
Prisoners in Research
Proposed Project Questionnaire
Protocol Deviation Policy (IBC)
Protocol Deviations (IRB)
Protocol Revision Policy
Recombinant DNA Research Questionnaire (RDRQ)
UPDATED
Recombinant DNA Research Questionnaire (RDRQ) for Core Services
Re-Consent and Notification
Reporting Requirements for IBC
Repository Policy for Human Subjects Research
Repository Protocol Checklist
Repository Questions for Non-OHSU Institutions
Repository Sharing Agreement (De-Identified)
Repository Sharing Agreement (Identifiable)
Repository Submittal Agreement
Repository Tracking Template EXCEL
Repository Tracking Template WORD
Representation Form for Research Involving Only Decedents' Information
Research Accidents and Spills
Research Involving Humans (Includes IRB authority, IRB procedures)
Research Involving Recombinant DNA
Responsible Conduct of Research & CoIR
Review Procedures Flowchart
Roles & Responsibilities in Research
Serious & Continuing Non-Compliance
Standards for Stereotactic Injection of Lentiviral Particles
State Laws and Regulations
Template Adenovirus Biosafety Manual
Template Biosafety Level 2 Manual
Template BSL 2+ Biosafety Manual
New
Template Lentivirus Biosafety Manual
Transgenic Animal Review Policy
Unanticipated Problems
Vaccinia Fact Sheet
NEW
Viral Vector Table
UPDATED
Waiver or Alteration of HIPAA Authorization
Waiver or Alteration of Informed Consent