Title
 | Description | Category
 |
|---|
Survey of Staff Use of Safety Medical Devices i
 |
Form |
IBC—Institutional Biosafety Committee |
Summary of NIH Guidlines for Research Involving Recombinant DNA Molecules
 |
Guidelines/Policies |
IBC—Institutional Biosafety Committee |
Summary of Guidelines for Research Involving Infectious Agents or Recombinant DNA Molecules
 |
Guidelines/Policies |
IBC—Institutional Biosafety Committee |
Subject Enrollment Logi
 |
Enrollment Log |
QAIP—Quality Assessment & Improvement Program |
Subject Eligibility Checklisti
 |
Eligibility Checklist |
QAIP—Quality Assessment & Improvement Program |
Study Team Signature and Delegation of Responsibility Logi
 |
Responsibility Log |
QAIP—Quality Assessment & Improvement Program |
Study Initiation Visit: Preventive Care for Your Study Site
 |
Education |
QAIP—Quality Assessment & Improvement Program |
Study Initiation Key Points
 |
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 |
QAIP—Quality Assessment & Improvement Program |
Student Work/Research Mentor Directory
 |
Student Summer Research List of Mentors and Supervisors |
Student Research |
Strategic Plan: Research Implementation Plan
 |
A detailed series of events required to strengthen and grow our research enterprise. |
Research Administration |
Strategic Plan for Strengthening Research
 |
This plan details SUNY Upstate's four research pillars and is the blueprint for the future. |
Research Administration |
Spanish Lanuage Standard Consent Sections
 |
Standard language for the 'In Case of Injury', 'Questions', and 'Voluntary Participation' sections |
IRB—Institutional Review Board (Human Subject) |
Spanish Language Version Signature Page Template
 |
Template |
IRB—Institutional Review Board (Human Subject) |
Site Visit Checklist i
 |
Checklist |
IBC—Institutional Biosafety Committee |
Signature Authorization Formi
 |
Post Awards document for PI to authorize funds |
Research Administration |
Security of Research Data: How to Protect Research Subjects
 |
Overview of relevant FDA guidelines, HIPAA Security, and State Law; best practices to follow for protecting electronic information |
IRB—Institutional Review Board (Human Subject) |
Sample Assent Form
 |
Form |
IRB—Institutional Review Board (Human Subject) |
Safety Product List
 |
List of safety products |
IBC—Institutional Biosafety Committee |
SOP for Obtaining Consent from Subjects who Enrolled as a Minor
 |
Guidelines/Policies |
IRB—Institutional Review Board (Human Subject) |
SOP for Establishing Legal Guardianship for Pediatric Subjects
 |
Guidelines/Policies |
IRB—Institutional Review Board (Human Subject) |