| Form Title | Form Category | Form 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 | |
| Mileage Reimbursement Form – FCC | 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 | |
| Fall 2004 | Newsletters | |
| Fall 2005 | Newsletters | |
| Fall 2006 | Newsletters | |
| Spring 2004 | Newsletters | |
| Spring 2005 | Newsletters | |
| Spring 2006 | Newsletters | |
| Spring 2007 | Newsletters | |
| Summer 2004 | Newsletters | |
| Summer 2007 | Newsletters | |
| Winter 2004 | Newsletters | |
| Winter 2005 | Newsletters |
Index to Forms