Newsletter Archives
Inside This Issue:
- Responsible Conduct of Research Training During Covid-19 Pandemic
- Tips for Presenting Scientific Images with Integrity
- USA's New Policy Library
- International Research: Considering Export Controls at the Proposal Stage
- Export License and Export Filing Requirements: Russia, China and Venezuela
- Working with Viral Vectors
- New Clinical Trials Webpage
- Investigational New Drug Guidance for Investigators
- Articles of Interest
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
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
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
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
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
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