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Human Subject Research - HSR
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HRPP/IRB Administration/Management and Process
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HRPP/IRB Administration/Management and Process
HRPP/IRB Administration/Management and Process
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17 - Third-Party Vendor Policy Awareness Program
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29 - The Non-human Subjects Research (NHSR) Application Review Process: Purposes and Benefits
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30 - Post Revised Common Rule Implementation: Risks of Maintaining an Institutional Review Board
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31 - Learning Ethics and Research Navigation: A Researcher-to-Researcher Approach
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32 - Successful Virtual IRB Meetings
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33 - Exploration of the Mutual Recognition Mechanism for Ethical Review in Chinese Oncology Clinical Trials
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36 - Navigating Ethical Terrain: IRB 101 in the AI Era
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37 - Navigating Ancillary Compliance Requirements During the IRB Review Process
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38 - Establishing a Human Research Protection Program SOP Process Within an Institution
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39 - ESTABLISHING AN INSTITUTIONAL SURVEY OFFICE FOR NAVIGATING DEPARTMENT OF DEFENSE SURVEY RESEARCH
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40 - Efforts to Streamline the IRB Reviews of Multicenter Clinical Trials in Japan
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41 - Implementing a Career Ladder for a Healthier Midsection
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42 - Single IRB Stakeholder Feedback: Evaluating the Use of the IRB Reliance Exchange
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43 - Improving Efficiencies in Single Institutional Review Board Reliance Processes Related to Informed Consent Development
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44 - Respect for the Reader: Language Sensitivity in Informed Consent Forms
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45 - Revising the IRB Submission Form: Lessons Learned From the Design Process
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46 - Benefits of Adding Informed Consent Specialists to an HRPP Program
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47 - Tracking non-Protocol Review-related HRPP activities
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48 - Building a National Working Group in Response to New AI/ML Ethical Challenges
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49 - Engaging Community in Human Research Protection Program (HRPP) Programming
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50 - Redesigning the Informed Consent - Future Use and Sharing Section
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51 - Balancing Open Science with Ethical Oversight: Challenges and Strategies for IRBs
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52 - Partnerships in Ethnography: Navigating IRB Processes with Transparency and Engagement
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53 - Balancing Act: Aligning IO Qualifications with Research Ethics Needs
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54 - Ethical Considerations of Artificial Intelligence (AI) Use in Research Settings
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55 - Development of Human Research Protection Programs in the Army
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56 - The Use of Artificial Intelligence in IRB Administration
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57 - Closing Time: Reconciling Lapsed Studies in an External IRB Portfolio
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58 - Evaluation of Virtual and In-person IRB Meetings During Calendar Year 2023 and 2024
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59 - Engaging IRB Chairs: Analysis of the Working Relationship of IRB Staff and Chairs prior to IRB Meetings
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60 - Reimagining IRB Rosters: Reducing Reviewer Burden amid a Growing Research Program
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91 - A one year review of enhancements to our Continuing Review Submission Process.
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92 - Streamlining Electronic Submission Systems: Navigating Customization Challenges and Transitioning to New Solutions
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97 - Enhancing IRB Interactions: Lessons Learned from the Hybrid Open Office Hours Program
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98 - Examining Withdrawal Rates and How Best to Mitigate Their Occurrences
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