Index to Forms
Form TitleForm CategoryForm Description
Absence from Work Form Employee Forms
Consultation Form Employee Forms
Education Reimbursement Form Employee Forms
Employee Reference Release Form Employee Forms
Mileage Reimbursement Form Employee Forms
Reimbursement Form Employee Forms
Sick Bank Donation Form Employee Forms
Travel Reimbursement Form Employee Forms
Travel Request Form Employee Forms
Disaster & Safety Policy and Procedures Employee Policies & Procedures
Education Reimbursement Policy Employee Policies & Procedures
Employee Handbook – East Coast Employee Policies & Procedures
Employee Handbook – West Coast Employee Policies & Procedures
Sick Bank Policy Employee Policies & Procedures
Mileage Reimbursement Form – FCC Investigator Forms
Sick Bank Donation Form Investigator Forms
Travel Request Form Investigator Forms
Travel Request Form – CA Investigator Forms
Authorship Guidelines Investigator Guidelines
Collaborating Investigator Guide Investigator Guidelines
Principal Investigator Orientation Guide Investigator Guidelines
Application for an Amendment (Change)/Addendum (New) IRB Grants Post-Approval
Application for Behavioral Study Review IRB Grants New Study/Initial Review Applications
Application for Bio-Medical Study Review IRB Grants New Study/Initial Review Applications
Application for Continuing Review IRB Grants Post-Approval
Application for Exemption from IRB Review IRB Grants New Study/Initial Review Applications
Application for Expedited Review IRB Grants New Study/Initial Review Applications
Application for Final Review IRB Grants Post-Approval
Deviation Form IRB Grants Post-Approval
Exempt Protocol Template IRB Grants Templates
Sample Assent Form IRB Grants Templates
Sample Informed Consent Document IRB Grants Templates
Serious Adverse Event (SAE)/Unanticipated Risk Report Form IRB Grants Post-Approval
Supplementary Application for Research Involving Children IRB Grants Supplementary Applications
Supplementary Application for Research Involving DNA/Tissue/Sample Banks IRB Grants Supplementary Applications
Supplementary Application for Research Involving Pregnant Women, Human Fetuses, and Neonates IRB Grants Supplementary Applications
Supplementary Application for Research Involving Prisoners IRB Grants Supplementary Applications
Supplementary Application: Indications for Investigational New Drug (IND) and Investigational Device Exemption (IDE) IRB Grants Supplementary Applications
Supplementary Application: Investigational Drug Information Record IRB Grants Supplementary Applications
Administrative Review and Distribution of Materials - IRB Policy 104.3 IRB Policies FUNCTIONS AND OPERATIONS
Advertisements - IRB Policy 107.1 IRB Policies INITIAL REVIEW CONSIDERATIONS
AIDS Related Research - IRB Policy 110.1 IRB Policies REVIEWS REQUIRING SPECIAL CONSIDERATION
Amendments or Addenda - IRB Policy 111.1 IRB Policies POST-IRB APPROVAL REVIEWS
Children - IRB Policy 109.3 IRB Policies VULNERABLE POPULATIONS
Collaborative Research - IRB Policy 106.1 IRB Policies COLLABORATIVE RESEARCH
Composition of the IRB - IRB Policy 103.1 IRB Policies IRB ORGANIZATION
Conflict of Interest - IRB Policy 102.1 IRB Policies CONFLICT OF INTEREST
Conflict of Interest in Research: Financial Disclosure Form IRB Policies Financial Disclosure Form
Continuing Reviews - IRB Policy 111.5 IRB Policies POST-IRB APPROVAL REVIEWS
Documentation and Document Management - IRB Policy 104.4 IRB Policies FUNCTIONS AND OPERATIONS
Duties of IRB Members - IRB Policy 103.3 IRB Policies IRB ORGANIZATION
Emergency Use of an Investigational Article - IRB Policy 105.3 IRB Policies TYPES OF IRB REVIEW
Exemptions from IRB Review - IRB Policy 105.2 IRB Policies TYPES OF IRB REVIEW
Expedited Review - IRB Policy 105.4 IRB Policies TYPES OF IRB REVIEW
Full Board Review - IRB Policy 105.5 IRB Policies TYPES OF IRB REVIEW
Genetic Research - IRB Policy 110.6 IRB Policies REVIEWS REQUIRING SPECIAL CONSIDERATION
Human Subjects Research - IRB Policy 105.1 IRB Policies TYPES OF IRB REVIEW
Informed Consent - IRB 108.1 IRB Policies INFORMED CONSENT
Initial Review Considerations - IRB Policy 107.1 IRB Policies INITIAL REVIEW CONSIDERATIONS
International Research - IRB Policy 110.2 IRB Policies REVIEWS REQUIRING SPECIAL CONSIDERATION
Investigational Use of Drugs and Biologics - IRB Policy 110.4 IRB Policies REVIEWS REQUIRING SPECIAL CONSIDERATION
IRB Communication and Notification - IRB Policy 113.1 IRB Policies IRB COMMUNICATION AND NOTIFICATION
IRB Meeting Administration - IRB Policy 104.2 IRB Policies FUNCTIONS AND OPERATIONS
Management of IRB Personnel - IRB Policy 101.3 IRB Policies GENERAL ADMINISTRATION
Management of the IRB - IRB Policy 103.2 IRB Policies IRB ORGANIZATION
Medical Devices - IRB Policy 110.3 IRB Policies REVIEWS REQUIRING SPECIAL CONSIDERATION
Policies and Procedures Maintenance - IRB Policy 101.1 IRB Policies GENERAL ADMINISTRATION
Post Approval Reporting IRB Policies IRB Guidance
Pregnant Women, Human Fetuses, and Neonates - IRB Policy 109.4 IRB Policies VULNERABLE POPULATIONS
Prisoners - IRB Policy 109.2 IRB Policies VULNERABLE POPULATIONS
Protocol Deviations - IRB Policy 111.4 IRB Policies POST-IRB APPROVAL REVIEWS
Quality Assurance - IRB Policy 115.1 IRB Policies QUALITY ASSURANCE
Research in Emergency Setting - IRB Policy 110.7 IRB Policies REVIEWS REQUIRING SPECIAL CONSIDERATION
Research Requiring the Use of Birth Control - IRB Policy 110.5 IRB Policies REVIEWS REQUIRING SPECIAL CONSIDERATION
Research Submission Requirements - IRB Policy 104.1 IRB Policies FUNCTIONS AND OPERATIONS
Responsibilities of Investigators - IRB Policy 114.1 IRB Policies RESPONSIBILITIES OF INVESTIGATORS
Serious Adverse Events and Unanticipated Problems - IRB Policy 111.2 IRB Policies POST-IRB APPROVAL REVIEWS
Signatory Authority - IRB Policy 101.4 IRB Policies GENERAL ADMINISTRATION
Significant New Findings - IRB Policy 111.3 IRB Policies POST-IRB APPROVAL REVIEWS
Statement of Authority and Purpose - IRB Policy 100.1 IRB Policies STATEMENT OF AUTHORITY AND PURPOSE
Study Close-Out - IRB Policy 112.1 IRB Policies STUDY CLOSE-OUT
Training and Education - IRB Policy 101.2 IRB Policies GENERAL ADMINISTRATION
Vulnerable Research Subjects - IRB Policy 109.1 IRB Policies VULNERABLE POPULATIONS
Conflict of Interest Policy IRB Resources Investigators
Scientific Misconduct Policy IRB Resources Investigators
State of California Requirements Pertaining to the Review of Human Subjects Research IRB Resources Investigators
State of Maryland Requirements Pertaining to the Review of Human Subjects Research IRB Resources Investigators
FCOI Policy Miscellaneous
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Summer 2004 Newsletters
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Winter 2004 Newsletters
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