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2020 Summer Newsletter
Dusty Layton and Angela Williams
Office of Research Compliance and Assurance Summer 2020 Newsletter.
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
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2019 Spring Newsletter
Dusty Layton and Angela Williams
Office of Research Compliance and Assurance Spring 2019 Newsletter.
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
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2018 Spring Newsletter
Dusty Layton and Angela Williams
Office of Research Compliance and Assurance Spring 2018 Newsletter.
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
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2018 Winter Newsletter
Dusty Layton and Angela Williams
Office of Research Compliance and Assurance Winter 2018 Newsletter.
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
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2017 Summer Newsletter
Dusty Layton and Angela Williams
Office of Research Compliance and Assurance 2017 Summer Newsletter.
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