2016
December: Regulatory Findings Documentation
November: Subject Recruitment
October: SOP 26 Recruitment Incentives
September: Privacy and Confidentiality
August: How to review and present protocols as the presenter
Accompanying documents:
- Reviewer checklist for initial applications
- Reviewer checklist for modifications
- Reviewer checklist for renewals
- Reviewer checklist – additional considerations
July: Re-Considerations
Accompanying document:
June: Re-consenting of Research Subjects
Accompanying documents:
- Clinical Research Regulatory Process – Understanding the Impact
- Changing Face of Clinical Trails – 1
- Informed Consent for New Investigators Editorial – Clinical Trials Series
May: How to Review Present Protocols as the Presenter
Accompanying documents:
- IRB Reviewer Checklist — Additional Considerations (2016 04 28)
- Online application reviewer checklist revised April 28 2016
April: Prisoners Quick Tip
March: Use of LARs in Research
February: Expanded Access HUD IRB Review
Accompanying document:
January: Short Form Consent Use