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