CITI Training Requirements
Conflict of Interest Management
Forms, Documents and Templates
(If you have difficulty accessing PDF files, please contact Research Administration Office at: 315 464-4323.)
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Document name beginning with the letter A. Number of document(s) found: 12
Note: i=interactive
Title
 | Description | Category
|
|---|---|---|
Access to Patient Information for Research Purposes: Demystifying the Process
 |
Educational Presentation | IRB—Institutional Review Board (Human Subject) |
Additional Study Personnel Form (Appendix A) i
 |
Personnel Form | IBC—Institutional Biosafety Committee |
| Adult & Minor Subjects Signature Page Template
|
Template | IRB—Institutional Review Board (Human Subject) |
| Adult Subjects Consent Template
|
Template | IRB—Institutional Review Board (Human Subject) |
| Adult Subjects Signature Page Template
|
Template | IRB—Institutional Review Board (Human Subject) |
| Adult and/or Minor Subjects Consent Template
|
Template | IRB—Institutional Review Board (Human Subject) |
| Advancing Clinical Research at Upstate-Investigator Training Program
|
an in-depth course for faculty who conduct human subject research | Research Administration |
| Adverse Event Guideline
|
Requirements for notifying the IRB of Unanticipated Events | IRB—Institutional Review Board (Human Subject) |
| Amended Informed Consent Regulations (FDA)
|
Amended informed consent regulations (FDA) | IRB—Institutional Review Board (Human Subject) |
| Application Form for Handling, Packaging and Shipping Blood, Tissue or Body Fluidsi
|
Application Form | IBC—Institutional Biosafety Committee |
| Application Form for Recombinant DNA, Bio-hazardous and Infectious Agent Researchi
|
Application Form | IBC—Institutional Biosafety Committee |
| Assessing Capacity to Consent for Research
|
Form | IRB—Institutional Review Board (Human Subject) |