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Document(s) in the category of IRB—Institutional Review Board (Human Subject). Number of document(s) found: 62
Note: i=interactive
Titleasc descDescriptionCategoryasc desc
"To Whom it May Concern" (Letter for Sponsors Regarding Adverse Events PDF document AE Letter for Spnsors 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)
Adult & Minor Subjects Signature Page Template Word document Template IRB—Institutional Review Board (Human Subject)
Adult Subjects Consent Template Word document Template 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)
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)
Assessing Capacity to Consent for Research Word document Form IRB—Institutional Review Board (Human Subject)
Banking Specimens Section Consent Template Word document Template IRB—Institutional Review Board (Human Subject)
Bosnian Language HIPAA Section Word document HIPAA section translated into Bosnian IRB—Institutional Review Board (Human Subject)
Bosnian Language Signature Pages Word document Signature pages translated into Bosnian IRB—Institutional Review Board (Human Subject)
Bosnian Language Standard Consent Sections Word document In Case of Injury, Questions, Voluntary Participation, etc. translated in to Bosnian IRB—Institutional Review Board (Human Subject)
CITI Education Requirement Policy PDF document Mandatory Human Subjects Education Program IRB—Institutional Review Board (Human Subject)
Case Reports Using Existing Data - Author Worksheeti Word document Case Report Guide IRB—Institutional Review Board (Human Subject)
Conflict of Interest Policy for IRB Members PDF document Guidelines/Policies IRB—Institutional Review Board (Human Subject)
Emergency Use Report Formi Word document Form IRB—Institutional Review Board (Human Subject)
Emergency Use of Unapproved Medical Devices PDF document Guidelines/Policies IRB—Institutional Review Board (Human Subject)
Emergency Use of an Investigational Drug or Biologic PDF document Guidelines/Policies IRB—Institutional Review Board (Human Subject)
FDA Guidance on Consent for the use of In Vitro Diagnostics PDF document Guidance IRB—Institutional Review Board (Human Subject)
FDA Guidance on In Vitro Diagnostics PDF document Guidance IRB—Institutional Review Board (Human Subject)
Genetic Testing & Banking Adults Consent Template Word document Template IRB—Institutional Review Board (Human Subject)
Genetic Testing & Banking Adults and Children Consent Template Word document Template IRB—Institutional Review Board (Human Subject)
Genetic Testing: Understanding Definitions and Key concepts PDF document Education IRB—Institutional Review Board (Human Subject)
Guidelines for Genetic Testing PDF document Guidelines/Policies IRB—Institutional Review Board (Human Subject)
Guidelines for Scientific Reviewers PDF document Guidelines/Policies IRB—Institutional Review Board (Human Subject)
HIPAA Required Section Consent Template Word document Template IRB—Institutional Review Board (Human Subject)
HIPAA Required Section Spanish Consent Template Word document Template IRB—Institutional Review Board (Human Subject)
HIPAA Review Prepatory to Research Request Form PDF document Form IRB—Institutional Review Board (Human Subject)
HIPAA and Research PDF document Guidelines/Policies IRB—Institutional Review Board (Human Subject)
How to Register for the CITI Basic or Refresher Course PDF document Step by step instructions on registering for the CITI Basic or Refresher Course IRB—Institutional Review Board (Human Subject)
IRBNet New User Registration and instruction document Word document IRBNet New User Registration and instructions IRB—Institutional Review Board (Human Subject)
IRBNet Training Energizer 1 PDF document IRBNet Training Energizer 1 IRB—Institutional Review Board (Human Subject)
IRBNet Training Energizer 2 PDF document IRBNet Training Energizer 2 IRB—Institutional Review Board (Human Subject)
In Vitro Diagnostocs Decision Tree PDF document Guidance IRB—Institutional Review Board (Human Subject)
Investigator 101 Education Material PDF document Education Material IRB—Institutional Review Board (Human Subject)
Investigator Responsibilities for Research Involving a Significant Risk Device PDF document Guidance IRB—Institutional Review Board (Human Subject)
Meeting Dates and Deadlines PDF document Dates and Deadlines IRB—Institutional Review Board (Human Subject)
Minor Subjects Only Signature Page Template Word document Template IRB—Institutional Review Board (Human Subject)
NCI CIRB Contact Information Word document Form IRB—Institutional Review Board (Human Subject)
NCI CIRB Study Closure Information Formi Word document Form IRB—Institutional Review Board (Human Subject)
NCI Central IRB (CIRB) Guidelines PDF document Guidelines/Policies IRB—Institutional Review Board (Human Subject)
Parental Permission Only Consent Template Word document Template IRB—Institutional Review Board (Human Subject)
Policy on IRB Review for Studies Pending Funding PDF document Policy IRB—Institutional Review Board (Human Subject)
Reporting of Protocol Deviations PDF document Protocol Deviation Policy IRB—Institutional Review Board (Human Subject)
Request Exemption from IRB Review PDF document Guidelines/Policies IRB—Institutional Review Board (Human Subject)
Request for Tissue for Research Purposes (Pathology Department Form)i Word document Form IRB—Institutional Review Board (Human Subject)
Requesting an IND Consult from the FDA PDF document Guidelines/Policies IRB—Institutional Review Board (Human Subject)
Research on Decedent's Information Requesti Word document Form IRB—Institutional Review Board (Human Subject)
SOP for Establishing Legal Guardianship for Pediatric Subjects PDF document Guidelines/Policies IRB—Institutional Review Board (Human Subject)
SOP for Obtaining Consent from Subjects who Enrolled as a Minor PDF document Guidelines/Policies IRB—Institutional Review Board (Human Subject)
Sample Assent Form Word document Form IRB—Institutional Review Board (Human Subject)
Security of Research Data: How to Protect Research Subjects PDF document Overview of relevant FDA guidelines, HIPAA Security, and State Law; best practices to follow for protecting electronic information IRB—Institutional Review Board (Human Subject)
Spanish Language Version Signature Page Template Word document Template IRB—Institutional Review Board (Human Subject)
Spanish Lanuage Standard Consent Sections Word document Standard language for the 'In Case of Injury', 'Questions', and 'Voluntary Participation' sections IRB—Institutional Review Board (Human Subject)
The Impact of The HIPAA Privacy Rule on Research PDF document Educational Presentation IRB—Institutional Review Board (Human Subject)
Unanticipated Problems and Adverse Event Flow Chart PDF document Determination Flow-chart IRB—Institutional Review Board (Human Subject)
University Hospital Patient Data Request Form PDF document Form IRB—Institutional Review Board (Human Subject)
University Hospital, Voluntary Faculty Request to Conduct Research which Requires the Use / Disclosure of IIHIi PDF document Form IRB—Institutional Review Board (Human Subject)
Upstate IRB Guidelines & Policies PDF document Guidelines/Policies IRB—Institutional Review Board (Human Subject)
Volunteer Recruitment Formi Word document Form IRB—Institutional Review Board (Human Subject)
Waiver of Authorization Request Formi Word document Form IRB—Institutional Review Board (Human Subject)