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Research Integrity
– Policies, Rules and Regulations
– Research Misconduct
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–– RCR Courses
–– RCR Frequently Asked Questions (FAQs)
–– RCR Training Notification Receipt
–– RCR Training: Authorized Course Completion Form
–– RCR Training: Authorized Course Enrollment Form
Conflicts of Interest (COI)
– Policies, Rules and Regulations
– Procedures and Guidance
– Conflicts in Research
– Conflict Management Guidance
– Notice of Intent (NOI)
– Training
Export Controls Office
– Policies, Rules and Regulations
–– Iran Sanctions
–– Restricted Party Screening
– Controlled Unclassified Information (CUI)
–– SURE Request
– Traveling Internationally / Attending Conferences
– Accepting Publication Restrictions in Research
– International Shipping
–– Export Control Determination Request
–– Know Your Recipient
– Hosting International Visitors
–– Visiting Scholar Questionnaire
– Online/Virtual Courses for Students Physically Outside the United States
– Working with International Staff and Students
– Conducting Research Outside the United States
–– EAR Temporary License Exceptions
– Training
Animal Care and Use (IACUC)
– Policies, Rules and Regulations
–– Animal Care and Use Statement
– Attending Veterinarian
––
Clinical Animal Health
Report
– Report Mistreatment or Noncompliance
– Procedures and Guidance
–– Administrative Review Procedures
–– Classification of Animal Use by Pain and Distress Categories
–– Disposition of Research and Teaching Animals
–– Guidance on Activities Requiring IACUC Approval
–– Guideline for Blanket Protocols
–– Needs for Prospective Clinical Studies Using Client-Owned Animals
–– Procedure for Semiannual Facility Inspections
–– Protocol and Amendment Review
–– Required Health/Medical Record Keeping for Research and Teaching Animals
–– Review Procedures for Significant Changes in an Approved Protocol
–– Tracking of Approval and Approved Animal Numbers
–– Use of Non-pharmaceutical-grade Compounds in Live Vertebrate Animals
–– Use of Restraint in Vertebrate Animal Studies
–– Veterinary Verification and Consultation (VVC) Reviews
– Forms and Templates
– Training
–– Animal Subjects Tutorial
Human Subjects (IRB)
– Policies, Rules and Regulations
– For Participants
– Procedures and Guidance
–– IRB: News
– Forms and Templates
–– Participant Concern and Complaint Form
–– Report Noncompliance Form
–– Report Unanticipated or Adverse Events Form
–– Request a Letter Form
–– Request a Group Education Event
–– Rush Request Form
– Cooperative Research
– Training
Definitions
Training
Anonymous Reporting
Directory
Request a Letter Form
Reason for request
*
Approval Letter – Exempt Study
Approval Letter – Expedited Study
Approval Letter – Full Board
.118 Determination Letter
Not Human Subjects Research (NHSR) Letter
PI Name
*
First
Last
PI NC State Email
*
PI Phone
*
Do you have a co-PI?
*
Yes
No
Name of co-PI
*
First
Last
Email for co-PI
*
Phone for co-PI
*
Institutional Affiliation
*
Protocol eIRB Number
*
Funding Source (if applicable)
*
Brief synopsis of your study’s purpose, the anticipated number and lived context of proposed participants, and your data collection methods.
*