2020 News and Announcements

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December 8, 2020

The IRB Review Newsletter [HTML]

In this issue:

  • UK CITI Access Link has moved
  • Office of Research Integrity (ORI) Holiday Schedule and Submission Deadlines
  • Reminder: Go to ORI's website to ensure you are using the most current documents and templates
  • New UK Electronic Research Notebook Website (previously LabArchives @ UK)
  • ORI Office Hours

Please note: Individuals conducting human subjects research must review and comply with the requirements of the VPR’s Resumption of Research Phased Plan before initiating or resuming any in-person research.


 

 

November 10, 2020

The IRB Review Newsletter [HTML]

In this issue:

  • UK CITI Access Link has moved
  • Office of Research Integrity (ORI) Thanksgiving Schedule
  • CCTS Clinical Research Update - Remote Informed Consent: The Same, but Different, but Still the Same presentation recording now available
  • LabArchives Overview & Demonstration Training Events
  • ORI Office Hours

Please note: Individuals conducting human subjects research must review and comply with the requirements of the VPR’s Resumption of Research Phased Plan before initiating or resuming any in-person research.


 

 

October 23, 2020

The IRB Review Newsletter [HTML]

In this issue:

  • FDA-Regulated Clinical Trials COVID-19 Guidance
  • LabArchives Overview & Demonstration Training Events
  • ORI Office Hours

Please note: Individuals conducting human subjects research must review and comply with the requirements of the VPR’s Resumption of Research Phased Plan before initiating or resuming any in-person research.


 

 

September 21, 2020

The IRB Review Newsletter [HTML]

In this issue:

  • Reminder to Submit Signed Consent Documents Not Attached to Continuing or Annual Review Submissions During Remote Work
  • Remote Monitoring of Clinical Trials Now Available
  • LabArchives Overview & Demonstration Training Events
  • ORI Office Hours

Please note: Individuals conducting human subjects research must review and comply with the requirements of the VPR’s Resumption of Research Phased Plan before initiating or resuming any in-person research.


 

 

August 12, 2020

The IRB Review Newsletter [HTML]

In this issue:

  • Expedited IRB Review for Individual Patient Compassionate Use
  • COVID-19 Human Research Protocols
  • Upcoming ORI Office Hours

Please note: Individuals conducting human subjects research must review and comply with the requirements of the VPR’s Resumption of Research Phased Plan before initiating or resuming any in-person research.


 

 

June 12, 2020

The IRB Review Newsletter [HTML]

In this issue: 

  • Applying the UK Resumption of Research Plan to Human Subject Research
  • Consolidated Guide for Submitting and Conducting COVID-19 Human Research
  • Revised "UK ORI Best Practice for Remote Informed Consent Guide"
  • IRB Member Spotlight: IRB Members Dr. Hay Avasarala and Dr. Avinash Bhakta featured in recent UKNOW articles
  • Upcoming ORI Office Hours

 

 

May 1, 2020

The IRB Review Newsletter [HTML]

In this issue:

  • COVID-19 Research Announcement
  • COVID-19 Informed Consent Options
  • NEW Online Training Opportunities!
  • Other Online Training Opportunities
  • Upcoming ORI Office Hours

 

 

January 22, 2020

The IRB Review Newsletter [HTML]

In this issue:

  • Revised Common Rule: Efficiencies Experienced
  • Road to Re-accreditation
  • Upcoming ORI Office Hours

January 20, 2020

Important Information

As of January 20, 2020, According to the Revised Common Rule’s Cooperative Research Provision (45 CFR 46.114), all institutions located in the United States that are engaged in cooperative research conducted or supported by a Common Rule department or agency must rely upon approval by a Single IRB for the portion of the research conducted in the United States. For further information, click here.