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Forms & Documents

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What is a Clinical Trial For Volunteers?
For use when negotiating a budget for Pharmacy Fees
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Institutions that receive support from Public Health Services offices and agencies, such as NIH, are responsible for following these policies to assure the responsible conduct of research and respond to allegations of research misconduct.
Policy describes ownership of data produced at Upstate by faculty, staff, students, fellows, etc.
An overview of regulatory and contractual policies that govern research and sponsored programs at Upstate and the Research Foundation of the State of New York.
This policy is based upon the ICMJE guidelines for granting authorship and contributorship
Biological Material Transfer, Uniform Biological Material Transfer Agreement Signatory
Uniform Biological Material Transfer Agreement Nonsignatory Agreement
Research Foundation Confidentiality Agreement
Standard Operating Procedures
Chemical Use Form
Guidelines/Policies
Guidelines/Policies
References
Checklist
Meeting Dates
Requirements for notifying the IRB of Unanticipated Events
Amended Informed Consent Regulations (FDA)
HIPAA section translated into Bosnian
In Case of Injury, Questions, Voluntary Participation, etc. translated in to Bosnian
Mandatory Human Subjects Education Program
Guidelines/Policies
Guidelines/Policies
Guidelines/Policies
Step by step instructions on registering for the CITI Basic or Refresher Course
Dates and Deadlines
IRBNet FAQs (Frequently Asked Questions)
IRBNet New User Registration and instructions
IRBNet Training Energizer 1
IRBNet Training Energizer 2
Education Material
Guidelines/Policies
Protocol Deviation Policy
Guidelines/Policies
Guidelines/Policies
Form
Overview of relevant FDA guidelines, HIPAA Security, and State Law; best practices to follow for protecting electronic information
Standard language for the 'In Case of Injury', 'Questions', and 'Voluntary Participation' sections
Educational Presentation
Guidelines/Policies
Application form and instructions for submission of bridge grants
Guidelines for eligibility and use of bridge grant funds
Application form and Instructions for Submission of Bridge Grants
Guidelines for eligibility and use of pilot grant funds
Informed Consent Checklist
Self-assessment Checklist
Note-to-File Form
Tips and Best Practices
QAIP Schematic
Key Points include: Informed Consent, Continuing Review Submission to the IRB, Confidentiality and HIPAA Issues, Amendments to Approved Protocols, Adverse Event Reporting to the IRB, Protocol Deviation Reporting to the IRB,DSMB Submission to the IRB
Eligibility Checklist
Enrollment Log
Prepare for Site Visit
an in-depth course for faculty who conduct human subject research
Fringe Benefit Rates for Fiscal Year 2021
Fee schedule for ust of Flow Cytometry Core Facility updated 2/2/10.
Checklist of important steps for grant application
Instructions for completing the Required Grant Request Form via Self-Serve when submitting a Grant.
Refresher requirements for RCR memo from Dave Amberg 9/2014
Fact sheet of Research Training Requirements through Citi.
Advanced Fluorescent Imaging Core Fee Schedule
Core Flow Aria Cell Sorter
Core Flow Cell Sorter
Fortessa Cell Analyzer
Flow
Core Flow Sort Questionaire
Core Flow Useful Links
Flow Core Fee Schedule
IHP MRI Core Policy January,2011 update
Use this form to request the services of the IHP MRI Core Research Facility
Application to request use of the Upstate Medical University Clinical Research Unit
core flow training
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