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Newsletter Archives

Summer 2020

Inside This Issue:

  • COVID-19 and Regulatory Research Activities 
  • When a Research Subject Cannot Physically
    Sign Informed Consent
  • Documenting the Informed Consent Process
  • Export Control Research 

Export Control Research 

Spring, 2019

Inside This Issue:

  • Human Subjects Research and Revised Common Rule
  • IRB Policies and Procedures
  • We Can Help By Speaking With Your Class About IRB
  • New Autoclave SOP
  • National Science Foundation Policy on Harassment
  • Responsible Conduct of Training Series is Still in Progress!
  • Hosting Visitors from Embargoed Countries
  • Items of Interest
  • Office of Research Compliance and Assurance: Committees and Programs

Summer, 2018

Inside This Issue:

  • 2018 Common Rule Burden-Reducing Provisions
  • IRBNet and Updated Feature: Human Subjects Research
  • Receiving/Purchasing Materials for Research?
  • Export Control: Quick Tips
  • New Biosafety Training Requirements
  • NSF Notice 144: Sexual Harassment
  • Reminder: Clinical Research Investigators: RCR Colloquia
  • Office of Research Integrity (ORI) Spring 2018 Newsletter
  • Food and Drug Administration: Research Subject Compensation
  • DHHS Office of Human Research Protections Workshop on Informed Consent 

Spring, 2018

Inside This Issue:

  • New Informed Consent Templates
  • Healthcare Operations:  Research vs. Quality Improvement
  • Update on Common Rule
  • New Export Control Training Module
  • Reminder:  NSF Responsible Conduct of Research Training Requirement 
  • Items of Interest 

Winter, 2018

Inside This Issue:

  • Common Rule 2018 Updates
  • Recap:  NIH Policy Changes
  • NIH Changes to Certificate of Confidentiality
  • NIH Policy:  Single IRB for Multi-Site Research Studies
  • 2017-2018 Responsible Conduct of Research Training Series
  • Updates and New Information

Summer, 2017

Inside This Issue:

  • IRB Submission:  Getting Started
  • Involvement in Clinical Research:  For Non-Healthcare Providers
  • Western IRB (WIRB) Submission Now Live
  • Clinical Research Fundamentals Training
  • Clinical Trials Module
  • Welcome New Staff
  • QA/QI Program
  • Observing Informed Consent Process
  • Conducting Research Responsibly:  Data Management Practices