OHSU

Research Integrity



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Title Policy Forms Add'l Info
Additional Consent Information for Different Types of Studies      
Advertising  
Alternative Sources of Information on Human Subjects Ethics      
Annual Event Summary Form    
Annual Renewal/Project Modification form    
Annual review policy
Appeal of Decisions Made by the Institutional Review Board      
Approval Timeframes - Service Level Understanding    
Approved and Unapproved Devices in Research    
Assent Form - Shriners    
Assent Form - Standard    
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    
Committee Charter    
Committee Member Reviewer Form    
Community Partnerships      
Compassionate and Expanded Use of Drugs and Devices      
Compensation for Research Participation      
Confidentiality of the Review Process      
Conflict of Interest in Research
Conflicts of Interest in Human Subjects Research - IRB Policy    
Consent for Special and Vulnerable Populations      
Consent Form    
Consent Form - Barcode    
Consent Form - Children's Oncology Group (COG) studies    
Consent Form - Consent and HIPAA  Authorization - Barcode    
Consent Form - Consent and HIPAA Authorization    
Consent Form - Gene Transfer    
Consent Form - Genetic    
Consent Form - Genetic Barcode    
Consent Form - Humanitarian Use Device    
Consent Form - Knight Cancer Institute    
Consent Form - Low Risk    
Consent Form - Media    
Consent Form - Shriners    
Consent Form- Repository Consent/Authorization  
Consent Form Signature Templates - Children Ages 15-17    
Consent Form, short - Arabic    
Consent Form, short - Chinese    
Consent Form, short - English translation    
Consent Form, short - Farsi    
Consent Form, short - German    
Consent Form, short - instructions for use    
Consent Form, short - Korean    
Consent Form, short - Russian    
Consent Form, short - Serbo-Croation    
Consent Form, short - Spanish    
Consent Form, short - Vietnamese    
Constituting the Institutional Review Board      
Consultants      
Continuing Review  
Coordinating Centers      
Core Services Recombinant DNA Research Questionnaire NEW  
Cost Language    
Costs Associated with Research Participation      
Data and Safety Monitoring
Data Use Agreement    
Decisionally Impaired Adults in Research  
Documentation of Informed Consent      
DSMP Template Form  
eIRB Hard Copy Submission    
eIRB System    
Electronic Signatures      
Elements of Informed Consent  
Emergency Single Time Use of a Test Article (Drug, Biologic, Device)    
Enrollment Incentives      
Exempt Review  
Expectations of IRB Membership      
Expedited Review  
Federal Wide Assurance (FWA)  
Finder's Fees      
Forms, IRB      
Full Board Review      
Functions and Responsibilities    
Genetic Research  
HIPAA Authorization for Obtaining Existing Records Outside of OHSU    
HIPAA Research Authorization    
HIPAA Research Authorization - Barcode     
HIPAA Research Authorization - Large Print    
HIPAA Research Authorization - Short Form    
HIPAA Research Authorization - Spanish    
HIV Testing      
Human Subjects Research in the Future    
Humanitarian Use Device (HUD)    
IBC Questionnaire for Human Subjects Studies Updated    
Individual Investigator Agreement (IIA)    
Infectious Agent/Toxin Questionnaire  
Information Sheet - HIV    
Informed Consent    
Initial Evaluation of Submitted Projects      
Initial Recombinant DNA Research Classification Form  
Initial Submission Guide    
Institutional Reporting Requirements      
International Research      
Investigational Drug Research    
IRB Authorization Agreement - Use this form when OHSU is accepting IRB oversight    
IRB Authorization Agreement - Use this form when OHSU is waiving IRB oversight    
IRB Chair's Advisory Committee (ICAC)      
IRB Minutes      
Knowledge of Local Context      
Lab Safety Manual    
Lay Language Protocol Summary    
Liability Language - Subject Injury  
Meetings      
Member Conflict of Interest policy    
Modifications    
Multi-Site Studies      
Non-Compliance with IRB Policies, Procedures, or Decisions    
Obtaining & Documenting Informed Consent From Subjects with Limited English Proficiency    
Obtaining Permission from Legally Authorized Representatives or Family Members      
Off Label Use of Drugs and Devices      
Off-Site Activities      
OHSU Students as Subjects    
PI Eligibility Policy    
Planned Emergency Research    
Pregnant Women, Human Fetuses, and Neonates in Research      
Prep to Research
Prisoners in Research    
Proposed Project Questionnaire    
Protocol Deviation Form    
Protocol Deviation Policy
Protocol Deviations    
Protocol Files      
Protocol Revision Policy
Purpose and Scope of Policies and Procedures      
Recombinant DNA Research Questionnaire  
Re-Consent and Notification    
Records Retention Requirements      
Recruitment of Research Participants      
Reporting Policy      
Reporting Requirements for IBC    
Repositories - Human Subjects Research Repository Policy  
Repositories - Non-OHSU Repository Questions    
Repositories - Repository Protocol Checklist    
Repositories - Repository Sharing Agreement (De-Identified)    
Repositories - Repository Sharing Agreement (Identifiable)    
Repositories - Repository Tracking Template EXCEL    
Repositories - Repository Tracking Template WORD    
Repositories - Submittal Agreement    
Representation Form for Research Involving Only Decedents' Information    
Required Training in Human Participants Ethics      
Requirements for Initial IRB Review      
Research Accidents and Spills
Research and HIPAA      
Research Determinations      
Research Development      
Research Involving Humans (Includes IRB authority, IRB procedures)    
Research Involving Recombinant DNA    
Research Oversight      
Research with Biologics      
Research with Kaiser      
Research with the Veterans Administration      
Responsible Conduct of Research & CoIR    
Review Procedures Flowchart    
Roles & Responsibilities in Research  
Selection of Institutional Review Board Chairs, Members and Staff      
Serious & Continuing Non-Compliance  
Standards for Stereotactic Injection of Lentiviral Particles    
State Laws and Regulations    
Stem Cell Research      
Student Research      
Students and Staff in Research      
Template Adenovirus Biosafety Manual    
Template Biosafety Level 2 Manual    
Template Lentivirus Biosafety Manual    
Training for IRB Members & IRB Chairs      
Training for ORIO Staff Members      
Transgenic Animal Review Policy
Unanticipated Problems
Waiver of Documentation of Informed Consent      
Waiver or Alteration of HIPAA Authorization    
Waiver or Alteration of Informed Consent  
Web Postings      
Women and Minorities in Research