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Advancing Clinical Research at Upstate-Investigator Training Program PDF document an in-depth course for faculty who conduct human subject research Research Administration
Adult & Minor Subjects Signature Page Template Word document Template IRB—Institutional Review Board (Human Subject)
Assessing Capacity to Consent for Research Word document Form IRB—Institutional Review Board (Human Subject)
Access to Patient Information for Research Purposes: Demystifying the Process PDF document Educational Presentation IRB—Institutional Review Board (Human Subject)
Adverse Event Guideline PDF document Requirements for notifying the IRB of Unanticipated Events IRB—Institutional Review Board (Human Subject)
Amended Informed Consent Regulations (FDA) PDF document Amended informed consent regulations (FDA) IRB—Institutional Review Board (Human Subject)
Adult Subjects Signature Page Template Word document Template IRB—Institutional Review Board (Human Subject)
Adult and/or Minor Subjects Consent Template Word document Template IRB—Institutional Review Board (Human Subject)
Adult Subjects Consent Template Word document Template IRB—Institutional Review Board (Human Subject)
Additional Study Personnel Form (Appendix A) i Word document Personnel Form IBC—Institutional Biosafety Committee
Application Form for Handling, Packaging and Shipping Blood, Tissue or Body Fluids i Word document Application Form IBC—Institutional Biosafety Committee
Application Form for Recombinant DNA, Bio-hazardous and Infectious Agent Researchi Word document Application Form IBC—Institutional Biosafety Committee