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Browse by Poster Presenter

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A
Abbass, Ibrahim

Genentech
5 - Integrating Social Determinants of Health (SDOH) into Clinical Trials: Feasibility Assessment, and Early Results
Ibrahim Abbass
Favorite
Abdi, Sepideh

BIDMC
7 - Addressing Anemia in Women: Proposals for Gender-Responsive Blood Draw Practices and Screening Protocols
Sepideh Abdi
Favorite
Adams, Jonathan

Emory University
101 - Customized Risk-Based Post-Approval Monitoring Sessions to Improve Animal Welfare Related Compliance
Jonathan Adams
Favorite
Adebamowo, Clement

Department of Epidemiology and Public Health, University of Maryland School of Medicine, Baltimore, MD, USA
93 - Perspectives of donor community on the use of anonymously collected, immortalized cells to create induced pluripotent stem cells (iPSC)
Clement Adebamowo
Favorite
99 - Scoping Review of the Ethical Regulations for Alzheimer’s Disease and Alzheimer’s Disease Related Dementia Research in Africa
Clement Adebamowo
Favorite
Adebamowo, Sally

Department of Epidemiology and Public Health, University of Maryland School of Medicine, Baltimore, MD, USA
93 - Perspectives of donor community on the use of anonymously collected, immortalized cells to create induced pluripotent stem cells (iPSC)
Sally Adebamowo
Favorite
Adedeji, Isaac

Center for Bioethics and Research, Ibadan, Oyo State, Nigeria
99 - Scoping Review of the Ethical Regulations for Alzheimer’s Disease and Alzheimer’s Disease Related Dementia Research in Africa
Isaac Adedeji
Favorite
Adekar, Sharad

WCG
2 - Use of Gender-inclusive Language in Subject Recruitment Materials and other Participant-Facing Documents in Clinical Trials
Sharad Adekar
Favorite
3 - Companion diagnostics medical devices in Clinical trials and their regulatory determinations, and experience of Independent IRB
Sharad Adekar
Favorite
4 - Risk mitigation Practices for Protection of Non-subjects in Human Gene Transfer Clinical Trials
Sharad Adekar
Favorite
Aguilera, Liz

NYU Langone Health
68 - Preliminary Results from the Development of a Quantification System for Reporting of Non-Compliance: An Impact Scoring System for Quality Assurance Report
Liz Aguilera
Favorite
Alborzi Avanaki, Mahsa

Department of Radiology, Beth Israel Deaconess Medical Center, Boston, MA, USA
7 - Addressing Anemia in Women: Proposals for Gender-Responsive Blood Draw Practices and Screening Protocols
Mahsa Alborzi Avanaki
Favorite
Ali, Mahnoor

Teachers College at Columbia University
54 - Ethical Considerations of Artificial Intelligence (AI) Use in Research Settings
Mahnoor Ali
Favorite
97 - Enhancing IRB Interactions: Lessons Learned from the Hybrid Open Office Hours Program
Mahnoor Ali
Favorite
Alvarado, Martha

Department of the Army/Office of the Surgeon General
63 - Post-Approval Compliance Monitoring in a Military Prison
Martha Alvarado
Favorite
Alvarez, Lisa

University of Texas at Arlington
56 - The Use of Artificial Intelligence in IRB Administration
Lisa Alvarez
Favorite
Anderson, Emily

Loyola University Chicago Stritch School of Medicine
14 - Characterization of Users of an Online Human Research Protections Training Program for Community Research Partners
Emily Anderson
Favorite
15 - Training Requirements for Community Research Partners at CTSA-funded Research Institutions
Emily Anderson
Favorite
Apostolova, Liana

Indiana University School of Medicine, Department of Neurology
76 - Ethical and Procedural Interplay between Ongoing Research Programs and Ancillary Studies
Liana Apostolova
Favorite
Ashat, Daniel

Oak Ridge Associated Universities
47 - Tracking non-Protocol Review-related HRPP activities
Daniel Ashat
Favorite
Astein, Diego

Advarra
64 - A LAR(ge) Problem: Review Approaches to Approving Enrollment of Adults Requiring Surrogate Consent
Diego Astein
Favorite
Atchison, Andrew

University of Alabama at Birmingham
41 - Implementing a Career Ladder for a Healthier Midsection
Andrew Atchison
Favorite
Attia, Shaza

Emirates College for Advanced Education
62 - A Systematic Review of Reported Assent Methodology in Early Childhood Research
Shaza Attia
Favorite
65 - A Survey of Researchers’ Experiences with Assent and Child Participants in Research
Shaza Attia
Favorite
B
Bacon, Kristin

University of Hawai‘i System Human Studies Program
49 - Engaging Community in Human Research Protection Program (HRPP) Programming
Kristin Bacon
Favorite
Bae, Diana

Columbia University
54 - Ethical Considerations of Artificial Intelligence (AI) Use in Research Settings
Diana Bae
Favorite
Bailey, Christopher

National Intelligence University
18 - IRB Review, Student Education
Christopher Bailey
Favorite
Ball, Margaret

University of Virginia
22 - Supporting Social, Behavioral and Educational Researchers with Study Compliance: Providing an on-demand tool for researchers to self-assess and to facilitate reaching out to the IRB-SBS for help.
Margaret Ball
Favorite
Basse, Galen

University of Washington
24 - IRB Pre-Review Tools Reduce Expedited Initial Application Median Turn-Around Times (mTAT)
Galen Basse
Favorite
Baumgartner, Angela

Northwestern University
71 - The NeverEnding Study: A Focused Post-Approval Monitoring Approach for Studies that Do Not Expire
Angela Baumgartner
Favorite
Belak, Mary

St. Jude Children's Research Hospital
43 - Improving Efficiencies in Single Institutional Review Board Reliance Processes Related to Informed Consent Development
Mary Belak
Favorite
Bendtsen, Kathrine

Saint Louis University
74 - Navigating Therapeutic Misconceptions: Understanding the Role of Providers
Kathrine Bendtsen
Favorite
Benhoff, Katelyn

Vanderbilt University Medical Center
42 - Single IRB Stakeholder Feedback: Evaluating the Use of the IRB Reliance Exchange
Katelyn Benhoff
Favorite
Biggar, Erin

MSKCC
91 - A one year review of enhancements to our Continuing Review Submission Process.
Erin Biggar
Favorite
Bird, Jessica

Intermountain Health
59 - Engaging IRB Chairs: Analysis of the Working Relationship of IRB Staff and Chairs prior to IRB Meetings
Jessica Bird
Favorite
60 - Reimagining IRB Rosters: Reducing Reviewer Burden amid a Growing Research Program
Jessica Bird
Favorite
Bird, Meyad

UT Southwestern Medical Center
36 - Navigating Ethical Terrain: IRB 101 in the AI Era
Meyad Bird
Favorite
Blackmon, Christina

University of Alabama at Birmingham
41 - Implementing a Career Ladder for a Healthier Midsection
Christina Blackmon
Favorite
Blackwood, Bronwyn

University of Virginia
22 - Supporting Social, Behavioral and Educational Researchers with Study Compliance: Providing an on-demand tool for researchers to self-assess and to facilitate reaching out to the IRB-SBS for help.
Bronwyn Blackwood
Favorite
Bogdan, Matthew

MSKCC
91 - A one year review of enhancements to our Continuing Review Submission Process.
Matthew Bogdan
Favorite
Bowling, Samantha

Virginia Tech
20 - Specialty Areas: Avoiding the Pitfall of Jack of All Trades, Masters of None in a Human Research Protection Program
Samantha Bowling
Favorite
Brackeen, Margie

Nationwide Children's Hospital
10 - Involving Transgender and Gender Diverse (TGD) Individuals in Research: A Collaborative Process Improvement Project
Margie Brackeen
Favorite
Bresnahan, Maureen

Saint Louis University
67 - Enhancing Research Integrity and Compliance: Implementation and Assessment of a Quality Assurance Program at an Integrated Research Institution
Maureen Bresnahan
Favorite
Brosseau, Elizabeth

Department of Veterans Affairs Cooperative Studies Program Boston Coordinating Center
100 - Development and Implementation of a Human Rights Committee to Facilitate a Participant-Centered Approach to Research
Elizabeth Brosseau
Favorite
Brotchie-Fine, CeCe

Novartis
81 - Compassion Fatigue and Compassion Satisfaction for Lab Animal Professionals: a program to bring Culture of Care to a global team
CeCe Brotchie-Fine
Favorite
Brower, Erin

WCG IRB
2 - Use of Gender-inclusive Language in Subject Recruitment Materials and other Participant-Facing Documents in Clinical Trials
Erin Brower
Favorite
Brown, Isabel

Genentech
5 - Integrating Social Determinants of Health (SDOH) into Clinical Trials: Feasibility Assessment, and Early Results
Isabel Brown
Favorite
Brown, Justin

Manager
78 - Facilitating Ethical Education Research: A Model Program for IRB Collaboration with New York City Department of Education
Justin Brown
Favorite
C
Caldwell, Christine

Indiana University
76 - Ethical and Procedural Interplay between Ongoing Research Programs and Ancillary Studies
Christine Caldwell
Favorite
Callahan, Michael

University of Michigan
61 - ClinicalTrials.gov Results Reporting Workshop
Michael Callahan
Favorite
Cambria, Roy

Memorial Sloan Kettering Cancer Center
44 - Respect for the Reader: Language Sensitivity in Informed Consent Forms
Roy Cambria
Favorite
91 - A one year review of enhancements to our Continuing Review Submission Process.
Roy Cambria
Favorite
Carroll-Scott, Amy

Drexel University
1 - Community Engagement Practices of Institutional Review Boards
Amy Carroll-Scott
Favorite
Chen, Tiffany

Vanderbilt University Medical Center
42 - Single IRB Stakeholder Feedback: Evaluating the Use of the IRB Reliance Exchange
Tiffany Chen
Favorite
Chiodini, Amber

Northwestern University
85 - Holding Out for Approval: Navigating Protocol Approval Holds Using Digital Organizational Tools
Amber Chiodini
Favorite
Chun, Jeeyoung

University of Kentucky
21 - Development of the K-12 Teacher and Support Staff Human Subjects Protection Training Course
Jeeyoung Chun
Favorite
Clary, Logan

Northwestern University
57 - Closing Time: Reconciling Lapsed Studies in an External IRB Portfolio
Logan Clary
Favorite
Clemons, Carly

MSKCC
91 - A one year review of enhancements to our Continuing Review Submission Process.
Carly Clemons
Favorite
Coffin, Tara

WCG
2 - Use of Gender-inclusive Language in Subject Recruitment Materials and other Participant-Facing Documents in Clinical Trials
Tara Coffin
Favorite
Comeau, Donnella

Mass General Brigham
7 - Addressing Anemia in Women: Proposals for Gender-Responsive Blood Draw Practices and Screening Protocols
Donnella Comeau
Favorite
Cooks, Marcella

Northwestern University
57 - Closing Time: Reconciling Lapsed Studies in an External IRB Portfolio
Marcella Cooks
Favorite
Czudak, Lauren

Northwestern University
85 - Holding Out for Approval: Navigating Protocol Approval Holds Using Digital Organizational Tools
Lauren Czudak
Favorite
D
Das, Dola

Cleveland Clinic
82 - IACUC post approval monitoring program – an essential quality control tool.
Dola Das
Favorite
Davis, Hannah

Advarra
9 - Addressing Diversity, Equity, and Inclusion in Clinical Trials
Hannah Davis
Favorite
Daymude, Thomas

Centers for Disease Control and Prevention (CDC)
95 - Effectiveness of a Virtual Training Program, 2023
Thomas Daymude
Favorite
DeCausey, Barbara

Virginia Tech
20 - Specialty Areas: Avoiding the Pitfall of Jack of All Trades, Masters of None in a Human Research Protection Program
Barbara DeCausey
Favorite
75 - Shedding Light on the Gray Area: Process Improvement in Exempt-Level Reviews
Barbara DeCausey
Favorite
Denison, Toni

Texas Tech University Health Sciences Center
28 - Implementing a Quality Improvement Review Board for Oversight of Non-Human Subjects Research Projects
Toni Denison
Favorite
Des Roches, Carrie

University of California, Berkeley
98 - Examining Withdrawal Rates and How Best to Mitigate Their Occurrences
Carrie Des Roches
Favorite
DiBella, Jacqueline

Department of Veterans Affairs Cooperative Studies Program Boston Coordinating Center
100 - Development and Implementation of a Human Rights Committee to Facilitate a Participant-Centered Approach to Research
Jacqueline DiBella
Favorite
DiLallo, Gillian

Genentech
5 - Integrating Social Determinants of Health (SDOH) into Clinical Trials: Feasibility Assessment, and Early Results
Gillian DiLallo
Favorite
Dilts, Natalie

Vanderbilt University Medical Center
42 - Single IRB Stakeholder Feedback: Evaluating the Use of the IRB Reliance Exchange
Natalie Dilts
Favorite
Dimitrijevic, Sanja

Cleveland Clinic
82 - IACUC post approval monitoring program – an essential quality control tool.
Sanja Dimitrijevic
Favorite
Dominguez, Yuliana

MSKCC
91 - A one year review of enhancements to our Continuing Review Submission Process.
Yuliana Dominguez
Favorite
Donnelly, Mary

University of Michigan
17 - Third-Party Vendor Policy Awareness Program
Mary Donnelly
Favorite
Doyle, Christopher

WCG
4 - Risk mitigation Practices for Protection of Non-subjects in Human Gene Transfer Clinical Trials
Christopher Doyle
Favorite
Doyle, Lacey

Virginia Tech
20 - Specialty Areas: Avoiding the Pitfall of Jack of All Trades, Masters of None in a Human Research Protection Program
Lacey Doyle
Favorite
75 - Shedding Light on the Gray Area: Process Improvement in Exempt-Level Reviews
Lacey Doyle
Favorite
Duenas, Devan

Seattle Children's Research Institute
23 - The ENVISION Project: Creating a values-oriented platform for informed consent.
Devan Duenas
Favorite
Dunlap, Jeremiah

Northwestern University
85 - Holding Out for Approval: Navigating Protocol Approval Holds Using Digital Organizational Tools
Jeremiah Dunlap
Favorite
Dunn, Keren

Cedars-Sinai Medical Center
70 - Measuring Compliance with Policy for Processing Planned Protocol Deviations
Keren Dunn
Favorite
80 - Using Research Electronic Data Capture (REDCap) to Modernize an Inspection Program
Keren Dunn
Favorite
E
Eberhardt, Jenessa

USC
92 - Streamlining Electronic Submission Systems: Navigating Customization Challenges and Transitioning to New Solutions
Jenessa Eberhardt
Favorite
Eckstein, Lisa

Bellberry Ltd
25 - Conceptualizing Human Research Ethics Committees as Regulatory Actors: Implications for Expectations and Practices
Lisa Eckstein
Favorite
Elliott, Tessa

University of Michigan
69 - Proactive Monitoring: ClinicalTrials.gov Registration and Results Reporting
Tessa Elliott
Favorite
Erickson, Eric

U.S. Army DEVCOM Aramaments Center
63 - Post-Approval Compliance Monitoring in a Military Prison
Eric Erickson
Favorite
Evans, Brandi

Virginia Tech
20 - Specialty Areas: Avoiding the Pitfall of Jack of All Trades, Masters of None in a Human Research Protection Program
Brandi Evans
Favorite
Evans, Nicholas

University of Massachusetts Lowell
90 - More Than a Checkbox: The Ethics of Dual-Use Research Policy Implementation in the Context of Institutional Compliance
Nicholas Evans
Favorite
F
Falvo-Eppers, Sarah

MSKCC
91 - A one year review of enhancements to our Continuing Review Submission Process.
Sarah Falvo-Eppers
Favorite
Fedewa, Joshua

University of Michigan
50 - Redesigning the Informed Consent - Future Use and Sharing Section
Joshua Fedewa
Favorite
Fogarty, Justin

NYU Langone Health
68 - Preliminary Results from the Development of a Quantification System for Reporting of Non-Compliance: An Impact Scoring System for Quality Assurance Report
Justin Fogarty
Favorite
Fogerty, Annemarie

Massachusetts General Hospital
7 - Addressing Anemia in Women: Proposals for Gender-Responsive Blood Draw Practices and Screening Protocols
Annemarie Fogerty
Favorite
Francisco, Stephanie

UT Southwestern Medical Center
36 - Navigating Ethical Terrain: IRB 101 in the AI Era
Stephanie Francisco
Favorite
G
Gabler, Sadie

University of Utah
8 - Does a dedicated research language services team increase enrollment and retention in Spanish speaking participants?
Sadie Gabler
Favorite
Gaskill, Brianna

Novartis
81 - Compassion Fatigue and Compassion Satisfaction for Lab Animal Professionals: a program to bring Culture of Care to a global team
Brianna Gaskill
Favorite
Gaucher, Tara

University of Virginia
22 - Supporting Social, Behavioral and Educational Researchers with Study Compliance: Providing an on-demand tool for researchers to self-assess and to facilitate reaching out to the IRB-SBS for help.
Tara Gaucher
Favorite
Gelinas, Luke

Advarra
23 - The ENVISION Project: Creating a values-oriented platform for informed consent.
Luke Gelinas
Favorite
George, Cynthia

Cystic Fibrosis Foundation
23 - The ENVISION Project: Creating a values-oriented platform for informed consent.
Cynthia George
Favorite
Gibson, Astoria

Teachers College, Columbia University
32 - Successful Virtual IRB Meetings
Astoria Gibson
Favorite
Gibson, Kainen

Department of Veterans Affairs Cooperative Studies Program Boston Coordinating Center
100 - Development and Implementation of a Human Rights Committee to Facilitate a Participant-Centered Approach to Research
Kainen Gibson
Favorite
Giles, Jennifer

Houston Methodist Hospital
46 - Benefits of Adding Informed Consent Specialists to an HRPP Program
Jennifer Giles
Favorite
Gill, Surinder

Emory University
86 - The importance of the Research Protocol Analyst (RPA) in the administrative pre-review as part of the animal care and use program quality assurance
Surinder Gill
Favorite
Gill, Vik

MSKCC
91 - A one year review of enhancements to our Continuing Review Submission Process.
Vik Gill
Favorite
Godfrey, Laura

Memorial Sloan Kettering Cancer Center
44 - Respect for the Reader: Language Sensitivity in Informed Consent Forms
Laura Godfrey
Favorite
Godina, Marina

NYU Langone Health
27 - Using a RedCap form as an RNI submission tool
Marina Godina
Favorite
Goldman, Jessica

Emory University
86 - The importance of the Research Protocol Analyst (RPA) in the administrative pre-review as part of the animal care and use program quality assurance
Jessica Goldman
Favorite
Grabic, Mirela

Saint Louis University
67 - Enhancing Research Integrity and Compliance: Implementation and Assessment of a Quality Assurance Program at an Integrated Research Institution
Mirela Grabic
Favorite
Greening, Lisa

University of Texas at Arlington
56 - The Use of Artificial Intelligence in IRB Administration
Lisa Greening
Favorite
Green-Jackson, Lavar

University of Michigan
17 - Third-Party Vendor Policy Awareness Program
Lavar Green-Jackson
Favorite
Griffin, Leola

Houston Methodist Hospital
46 - Benefits of Adding Informed Consent Specialists to an HRPP Program
Leola Griffin
Favorite
Growcott, Ellena

Novartis
81 - Compassion Fatigue and Compassion Satisfaction for Lab Animal Professionals: a program to bring Culture of Care to a global team
Ellena Growcott
Favorite
Guyton, Amanda

University of Washington
24 - IRB Pre-Review Tools Reduce Expedited Initial Application Median Turn-Around Times (mTAT)
Amanda Guyton
Favorite
H
Hahn, Ryan

Novartis
81 - Compassion Fatigue and Compassion Satisfaction for Lab Animal Professionals: a program to bring Culture of Care to a global team
Ryan Hahn
Favorite
Haley, Alyssa

Cedars-Sinai Medical Center
70 - Measuring Compliance with Policy for Processing Planned Protocol Deviations
Alyssa Haley
Favorite
Hammers, Dustin
76 - Ethical and Procedural Interplay between Ongoing Research Programs and Ancillary Studies
Dustin Hammers
Favorite
Handy, Kelly

University of Texas at Arlington
56 - The Use of Artificial Intelligence in IRB Administration
Kelly Handy
Favorite
Harris, DeMoncheri

Centers for Disease Control and Prevention (CDC)
95 - Effectiveness of a Virtual Training Program, 2023
DeMoncheri Harris
Favorite
Hastings Truelove, Amber

Queen's University
96 - Needs and Preferences of Research Ethics Board Members in the Development of a New TCPS 2 Training Program in Canada
Amber Hastings Truelove
Favorite
Hayes, Wendy

St. Jude Children's Research Hospital
43 - Improving Efficiencies in Single Institutional Review Board Reliance Processes Related to Informed Consent Development
Wendy Hayes
Favorite
Heath, Tamika

Centers for Disease Control and Prevention (CDC)
95 - Effectiveness of a Virtual Training Program, 2023
Tamika Heath
Favorite
Helwani, Lubabah

University of Southern California
26 - What It Means to Conduct Belmont-Centric IRB Reviews
Lubabah Helwani
Favorite
92 - Streamlining Electronic Submission Systems: Navigating Customization Challenges and Transitioning to New Solutions
Lubabah Helwani
Favorite
Henriquez Taveras, Yefrenia

Teachers College, Columbia University & University of New England
32 - Successful Virtual IRB Meetings
Yefrenia Henriquez Taveras
Favorite
51 - Balancing Open Science with Ethical Oversight: Challenges and Strategies for IRBs
Yefrenia Henriquez Taveras
Favorite
52 - Partnerships in Ethnography: Navigating IRB Processes with Transparency and Engagement
Yefrenia Henriquez Taveras
Favorite
53 - Balancing Act: Aligning IO Qualifications with Research Ethics Needs
Yefrenia Henriquez Taveras
Favorite
54 - Ethical Considerations of Artificial Intelligence (AI) Use in Research Settings
Yefrenia Henriquez Taveras
Favorite
Howard, Kathleen

Department of Veterans Affairs Cooperative Studies Program Boston Coordinating Center
100 - Development and Implementation of a Human Rights Committee to Facilitate a Participant-Centered Approach to Research
Kathleen Howard
Favorite
Huang, Sabrina

Teachers College, Columbia University
52 - Partnerships in Ethnography: Navigating IRB Processes with Transparency and Engagement
Sabrina Huang
Favorite
Hunsche, Katy

University of Michigan
69 - Proactive Monitoring: ClinicalTrials.gov Registration and Results Reporting
Katy Hunsche
Favorite
Hwang, Elsa

Memorial Sloan Kettering Cancer Center
44 - Respect for the Reader: Language Sensitivity in Informed Consent Forms
Elsa Hwang
Favorite
I
Ibebunjo, Chikwendu

Novartis
81 - Compassion Fatigue and Compassion Satisfaction for Lab Animal Professionals: a program to bring Culture of Care to a global team
Chikwendu Ibebunjo
Favorite
Ikhane, Peter

Department of Epidemiology and Public Health, University of Maryland School of Medicine, Baltimore, MD, USA
93 - Perspectives of donor community on the use of anonymously collected, immortalized cells to create induced pluripotent stem cells (iPSC)
Peter Ikhane
Favorite
Inano, Akihiro

Fukushima Medical University / ACTIVATO
40 - Efforts to Streamline the IRB Reviews of Multicenter Clinical Trials in Japan
Akihiro Inano
Favorite
J
Jacobik, Beverly

University of Nevada, Las Vegas
45 - Revising the IRB Submission Form: Lessons Learned From the Design Process
Beverly Jacobik
Favorite
Jegede, Ayodele

Center for Bioethics and Research, Ibadan, Oyo State, Nigeria
99 - Scoping Review of the Ethical Regulations for Alzheimer’s Disease and Alzheimer’s Disease Related Dementia Research in Africa
Ayodele Jegede
Favorite
Jenkins, Andrea

University of Michigan
69 - Proactive Monitoring: ClinicalTrials.gov Registration and Results Reporting
Andrea Jenkins
Favorite
Jeschke-Lopez, Ikoa

NYU Langone Health
27 - Using a RedCap form as an RNI submission tool
Ikoa Jeschke-Lopez
Favorite
68 - Preliminary Results from the Development of a Quantification System for Reporting of Non-Compliance: An Impact Scoring System for Quality Assurance Report
Ikoa Jeschke-Lopez
Favorite
Johnson, Nadia

NYU Langone Health
27 - Using a RedCap form as an RNI submission tool
Nadia Johnson
Favorite
Joseph, Yonnette

NYU Langone Health
27 - Using a RedCap form as an RNI submission tool
Yonnette Joseph
Favorite
K
Kalbeitzer, Michelle

Emory University
48 - Building a National Working Group in Response to New AI/ML Ethical Challenges
Michelle Kalbeitzer
Favorite
Kaldor, Jenny

Public Health Services, Tasmanian Department of Heath
25 - Conceptualizing Human Research Ethics Committees as Regulatory Actors: Implications for Expectations and Practices
Jenny Kaldor
Favorite
Kaley, Thomas

MSKCC
91 - A one year review of enhancements to our Continuing Review Submission Process.
Thomas Kaley
Favorite
Kane, Monica

Northwestern University
57 - Closing Time: Reconciling Lapsed Studies in an External IRB Portfolio
Monica Kane
Favorite
Karlebach, Shara

Emory University
48 - Building a National Working Group in Response to New AI/ML Ethical Challenges
Shara Karlebach
Favorite
Keefer, Susan

University of Kentucky
21 - Development of the K-12 Teacher and Support Staff Human Subjects Protection Training Course
Susan Keefer
Favorite
Keeley, Abby

Washington University School of Medicine
19 - Maintaining a Virtual Presence with a Fully Remote HRPO
Abby Keeley
Favorite
66 - Addressing Barriers to Sustained Monitoring
Abby Keeley
Favorite
Kelly, Michelle

Emirates College for Advanced Education
62 - A Systematic Review of Reported Assent Methodology in Early Childhood Research
Michelle Kelly
Favorite
65 - A Survey of Researchers’ Experiences with Assent and Child Participants in Research
Michelle Kelly
Favorite
Kendrick, Kelsey

Cedars-Sinai Medical Center
80 - Using Research Electronic Data Capture (REDCap) to Modernize an Inspection Program
Kelsey Kendrick
Favorite
Kerby, Patricia

St. Jude Children's Research Hospital
43 - Improving Efficiencies in Single Institutional Review Board Reliance Processes Related to Informed Consent Development
Patricia Kerby
Favorite
Keriazes, Georgia

Lakeland Regional Health
73 - A Descriptive Assessment of Medical Chart Review Templates and their Requirements for Elements of Sound Research Design.
Georgia Keriazes
Favorite
Kester, Larry

EDO for Army Corrections Command
63 - Post-Approval Compliance Monitoring in a Military Prison
Larry Kester
Favorite
Khan, Yasmeen

Northwestern University
71 - The NeverEnding Study: A Focused Post-Approval Monitoring Approach for Studies that Do Not Expire
Yasmeen Khan
Favorite
Kirby, Kala

Indiana University School of Medicine, Department of Neurology
76 - Ethical and Procedural Interplay between Ongoing Research Programs and Ancillary Studies
Kala Kirby
Favorite
Kisenwether, Jessica

NASA Office of Research Assurance and Weill Cornell Medicine
53 - Balancing Act: Aligning IO Qualifications with Research Ethics Needs
Jessica Kisenwether
Favorite
Kiss, Jody

Cleveland Clinic
82 - IACUC post approval monitoring program – an essential quality control tool.
Jody Kiss
Favorite
Knasel, Rita

Northwestern University
57 - Closing Time: Reconciling Lapsed Studies in an External IRB Portfolio
Rita Knasel
Favorite
Koehl-Carabetta, Kristin

Novartis
81 - Compassion Fatigue and Compassion Satisfaction for Lab Animal Professionals: a program to bring Culture of Care to a global team
Kristin Koehl-Carabetta
Favorite
Komosamerle, Jena

Northwestern University
83 - Maintaining & Managing Satellite Facilities- How IACUCs Can Provide Necessary & Succinct Oversight with a Daily Activity Sheet
Jena Komosamerle
Favorite
Kraft, Stephanie

Geisinger College of Health Sciences
23 - The ENVISION Project: Creating a values-oriented platform for informed consent.
Stephanie Kraft
Favorite
Krishnamurti, Tamar

University of Pittsburgh
23 - The ENVISION Project: Creating a values-oriented platform for informed consent.
Tamar Krishnamurti
Favorite
L
Lafauce, Erica

Novartis
81 - Compassion Fatigue and Compassion Satisfaction for Lab Animal Professionals: a program to bring Culture of Care to a global team
Erica Lafauce
Favorite
Larkey, Matthew

NYU Langone Health
68 - Preliminary Results from the Development of a Quantification System for Reporting of Non-Compliance: An Impact Scoring System for Quality Assurance Report
Matthew Larkey
Favorite
Larson, Elaine

Columbia University in the City of New York; NY Academy of Medicine
58 - Evaluation of Virtual and In-person IRB Meetings During Calendar Year 2023 and 2024
Elaine Larson
Favorite
Lehmbeck, Jane

University of Virginia
22 - Supporting Social, Behavioral and Educational Researchers with Study Compliance: Providing an on-demand tool for researchers to self-assess and to facilitate reaching out to the IRB-SBS for help.
Jane Lehmbeck
Favorite
Leon, Finn

Teachers Colllege, Columbia University
78 - Facilitating Ethical Education Research: A Model Program for IRB Collaboration with New York City Department of Education
Finn Leon
Favorite
Leon, Vidal

Emory University
86 - The importance of the Research Protocol Analyst (RPA) in the administrative pre-review as part of the animal care and use program quality assurance
Vidal Leon
Favorite
Lieland, Stefanie

University of Michigan
69 - Proactive Monitoring: ClinicalTrials.gov Registration and Results Reporting
Stefanie Lieland
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Liu, Ruishuang

Peking University
11 - Patients attitudes towards the sharing of electronic health records for medical research
Ruishuang Liu
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Lubag, Daisy

University of California, Berkeley
37 - Navigating Ancillary Compliance Requirements During the IRB Review Process
Daisy Lubag
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Luery, Sarah

University of Southern California
26 - What It Means to Conduct Belmont-Centric IRB Reviews
Sarah Luery
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Luna, Angela

University of Texas at Arlington
56 - The Use of Artificial Intelligence in IRB Administration
Angela Luna
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Luna-Lucero, Myra

Teachers College, Columbia University
31 - Learning Ethics and Research Navigation: A Researcher-to-Researcher Approach
Myra Luna-Lucero
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32 - Successful Virtual IRB Meetings
Myra Luna-Lucero
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78 - Facilitating Ethical Education Research: A Model Program for IRB Collaboration with New York City Department of Education
Myra Luna-Lucero
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97 - Enhancing IRB Interactions: Lessons Learned from the Hybrid Open Office Hours Program
Myra Luna-Lucero
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Lynch, Lorena

Naval Health Research Center
38 - Establishing a Human Research Protection Program SOP Process Within an Institution
Lorena Lynch
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39 - ESTABLISHING AN INSTITUTIONAL SURVEY OFFICE FOR NAVIGATING DEPARTMENT OF DEFENSE SURVEY RESEARCH
Lorena Lynch
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Mal, AnneMarie

Baystate Medical Center
12 - Emotional Intelligence and the IRB
AnneMarie Mal
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Maril, Robert

NYU Langone Health
27 - Using a RedCap form as an RNI submission tool
Robert Maril
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Marlin, Susan

Clinical Trials Ontario
96 - Needs and Preferences of Research Ethics Board Members in the Development of a New TCPS 2 Training Program in Canada
Susan Marlin
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Massengill, David

Memorial Sloan Kettering Cancer Center
44 - Respect for the Reader: Language Sensitivity in Informed Consent Forms
David Massengill
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Mazuera, Sylvia

Cystic Fibrosis Foundation
23 - The ENVISION Project: Creating a values-oriented platform for informed consent.
Sylvia Mazuera
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McClintock, Adam

University of Alabama at Birmingham
41 - Implementing a Career Ladder for a Healthier Midsection
Adam McClintock
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McDonough, Tara

Army Human Research Protection Office (AHRPO)
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Tara McDonough
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McGregor, Muriel

University of Nevada, Las Vegas
45 - Revising the IRB Submission Form: Lessons Learned From the Design Process
Muriel McGregor
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McNair, Steven

Morehouse School of Medicine
88 - Advancing Diversity in Clinical Research through the Clinical Research Coordinator Certificate (CRCC) Program
Steven McNair
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Seattle Children's Research Institute
23 - The ENVISION Project: Creating a values-oriented platform for informed consent.
Sharon McNamara
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Northwestern University
85 - Holding Out for Approval: Navigating Protocol Approval Holds Using Digital Organizational Tools
Kelly McPartland
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Mead Jasperse, Sarah

Emirates College for Advanced Education
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Sarah Mead Jasperse
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65 - A Survey of Researchers’ Experiences with Assent and Child Participants in Research
Sarah Mead Jasperse
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Mendoza-Carvantes, Diana

Johns Hopkins Berman Institute of Bioethics, Baltimore, Maryland
99 - Scoping Review of the Ethical Regulations for Alzheimer’s Disease and Alzheimer’s Disease Related Dementia Research in Africa
Diana Mendoza-Carvantes
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Meyer, Esmeralda

Emory University
86 - The importance of the Research Protocol Analyst (RPA) in the administrative pre-review as part of the animal care and use program quality assurance
Esmeralda Meyer
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101 - Customized Risk-Based Post-Approval Monitoring Sessions to Improve Animal Welfare Related Compliance
Esmeralda Meyer
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Miladinovich, Stacy

University of California, Berkeley
98 - Examining Withdrawal Rates and How Best to Mitigate Their Occurrences
Stacy Miladinovich
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North Star Review Board
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Heather Miller
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Queen's University
96 - Needs and Preferences of Research Ethics Board Members in the Development of a New TCPS 2 Training Program in Canada
Miranda Miller
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Minder, Carissa

Washington University in St. Louis
77 - Is this Single IRB in Disguise?
Carissa Minder
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Minnock, Jack

University of Utah
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Mischler, James

Northwestern State University of Louisiana
29 - The Non-human Subjects Research (NHSR) Application Review Process: Purposes and Benefits
James Mischler
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Molina, Elizabeth

University of Michigan
16 - Participant Payments and Undue Influence
Elizabeth Molina
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Mongeon, Brianne

USC
92 - Streamlining Electronic Submission Systems: Navigating Customization Challenges and Transitioning to New Solutions
Brianne Mongeon
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Morais, John

Army Human Research Protections Office
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John Morais
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NYU Langone Health
27 - Using a RedCap form as an RNI submission tool
Frederick More
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Morningstar, Kirstin

University of Texas at Arlington
56 - The Use of Artificial Intelligence in IRB Administration
Kirstin Morningstar
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Moyer, Julie

Washington University in St. Louis
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Julie Moyer
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Mrdjenovich, Adam

University of Michigan
16 - Participant Payments and Undue Influence
Adam Mrdjenovich
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University of Pennsylvania
23 - The ENVISION Project: Creating a values-oriented platform for informed consent.
Rebecca Mueller
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Musema, Jane
76 - Ethical and Procedural Interplay between Ongoing Research Programs and Ancillary Studies
Jane Musema
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Nadim, Hend

UT Southwestern Medical Center
36 - Navigating Ethical Terrain: IRB 101 in the AI Era
Hend Nadim
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Nash, Carmen

Emory University
101 - Customized Risk-Based Post-Approval Monitoring Sessions to Improve Animal Welfare Related Compliance
Carmen Nash
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Neelon, Jennifer

University of Nevada, Las Vegas
45 - Revising the IRB Submission Form: Lessons Learned From the Design Process
Jennifer Neelon
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Ngo, Phi

Naval Health Research Center
38 - Establishing a Human Research Protection Program SOP Process Within an Institution
Phi Ngo
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39 - ESTABLISHING AN INSTITUTIONAL SURVEY OFFICE FOR NAVIGATING DEPARTMENT OF DEFENSE SURVEY RESEARCH
Phi Ngo
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Nguyen, Victoria

Alberta Health Services
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Victoria Nguyen
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65 - A Survey of Researchers’ Experiences with Assent and Child Participants in Research
Victoria Nguyen
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O'Brien, Jaime

University of Massachusetts Lowell
90 - More Than a Checkbox: The Ethics of Dual-Use Research Policy Implementation in the Context of Institutional Compliance
Jaime O'Brien
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Odor, Erin

Advarra
64 - A LAR(ge) Problem: Review Approaches to Approving Enrollment of Adults Requiring Surrogate Consent
Erin Odor
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Oilepo, Rhonda

UT Southwestern Medical Center
36 - Navigating Ethical Terrain: IRB 101 in the AI Era
Rhonda Oilepo
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O'Reilly, Eileen

MSKCC
91 - A one year review of enhancements to our Continuing Review Submission Process.
Eileen O'Reilly
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Owens, Shemetra

Baystate Medical Center
12 - Emotional Intelligence and the IRB
Shemetra Owens
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Panageas, Helen

NYU Langone Health
27 - Using a RedCap form as an RNI submission tool
Helen Panageas
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Payne, Jennifer

Queen's University
96 - Needs and Preferences of Research Ethics Board Members in the Development of a New TCPS 2 Training Program in Canada
Jennifer Payne
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Peachey, Neal

Cleveland Clinic
82 - IACUC post approval monitoring program – an essential quality control tool.
Neal Peachey
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Pemu, Priscilla

Morehouse School of Medicine
88 - Advancing Diversity in Clinical Research through the Clinical Research Coordinator Certificate (CRCC) Program
Priscilla Pemu
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Pena, Anthony

Sage Bionetworks
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Anthony Pena
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Peterson, James

Centers for Disease Control and Prevention (CDC)
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James Peterson
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Phillips, Hannah

Nationwide Children's Hospital
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Hannah Phillips
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Phung, Elizabeth

Novartis
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Elizabeth Phung
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Plew, Sarah

University of Texas at Arlington
56 - The Use of Artificial Intelligence in IRB Administration
Sarah Plew
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Porter, Kathryn

Seattle Children's Research Institute
23 - The ENVISION Project: Creating a values-oriented platform for informed consent.
Kathryn Porter
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Pottenger, Amy

Indiana University School of Medicine, Department of Neurology
76 - Ethical and Procedural Interplay between Ongoing Research Programs and Ancillary Studies
Amy Pottenger
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R
Ramiro, Joy

University of Nevada, Las Vegas
45 - Revising the IRB Submission Form: Lessons Learned From the Design Process
Joy Ramiro
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Randall, Catherine

Memorial Sloan Kettering Cancer Center
44 - Respect for the Reader: Language Sensitivity in Informed Consent Forms
Catherine Randall
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Rentcome, Jessica

Houston Methodist Hospital
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Jessica Rentcome
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Riffle, Rachelle

Intermountain Health
59 - Engaging IRB Chairs: Analysis of the Working Relationship of IRB Staff and Chairs prior to IRB Meetings
Rachelle Riffle
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60 - Reimagining IRB Rosters: Reducing Reviewer Burden amid a Growing Research Program
Rachelle Riffle
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Memorial Sloan Kettering Cancer Center
44 - Respect for the Reader: Language Sensitivity in Informed Consent Forms
Ann Rodavitch
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91 - A one year review of enhancements to our Continuing Review Submission Process.
Ann Rodavitch
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Rotterman, Briana

Emory University
48 - Building a National Working Group in Response to New AI/ML Ethical Challenges
Briana Rotterman
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Rousselle, Rebecca

Emory University
48 - Building a National Working Group in Response to New AI/ML Ethical Challenges
Rebecca Rousselle
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Rozynska, Joanna

University of Warsaw, Poland
94 - Ethical payment to research participants: a principle-based analysis
Joanna Rozynska
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Ruhsam, Andrea

University of Virginia
22 - Supporting Social, Behavioral and Educational Researchers with Study Compliance: Providing an on-demand tool for researchers to self-assess and to facilitate reaching out to the IRB-SBS for help.
Andrea Ruhsam
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Rule, Sarah

Department of the Army
63 - Post-Approval Compliance Monitoring in a Military Prison
Sarah Rule
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Ruotolo, Brenda

Columbia University in the City of New York
58 - Evaluation of Virtual and In-person IRB Meetings During Calendar Year 2023 and 2024
Brenda Ruotolo
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Rusgo, Allison

Drexel University
1 - Community Engagement Practices of Institutional Review Boards
Allison Rusgo
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Sagar, Ajay

Cedars-Sinai Medical Center
80 - Using Research Electronic Data Capture (REDCap) to Modernize an Inspection Program
Ajay Sagar
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Sanchez, Hayley

Sage Bionetworks
72 - A Landscape Survey of Generalist Data Repositories to Facilitate Researcher Selection and IRB Review
Hayley Sanchez
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Santiago, Alison

Center for Clinical and Translational Science
14 - Characterization of Users of an Online Human Research Protections Training Program for Community Research Partners
Alison Santiago
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15 - Training Requirements for Community Research Partners at CTSA-funded Research Institutions
Alison Santiago
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Sasamoto, Kate

University of Michigan
69 - Proactive Monitoring: ClinicalTrials.gov Registration and Results Reporting
Kate Sasamoto
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Savage, Maria

University of Washington
24 - IRB Pre-Review Tools Reduce Expedited Initial Application Median Turn-Around Times (mTAT)
Maria Savage
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Seabolt, Brian

University Of Michigan
50 - Redesigning the Informed Consent - Future Use and Sharing Section
Brian Seabolt
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Seabrooke, Lee

Saint Louis University
67 - Enhancing Research Integrity and Compliance: Implementation and Assessment of a Quality Assurance Program at an Integrated Research Institution
Lee Seabrooke
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Serdoz, Emily

Vanderbilt University Medical Center
42 - Single IRB Stakeholder Feedback: Evaluating the Use of the IRB Reliance Exchange
Emily Serdoz
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Shiferaw, Ayalnesh

Emory University
86 - The importance of the Research Protocol Analyst (RPA) in the administrative pre-review as part of the animal care and use program quality assurance
Ayalnesh Shiferaw
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Showkat, Nazaf

Novartis
81 - Compassion Fatigue and Compassion Satisfaction for Lab Animal Professionals: a program to bring Culture of Care to a global team
Nazaf Showkat
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Sicilia, Rosmery

Department of Veterans Affairs Cooperative Studies Program Boston Coordinating Center
100 - Development and Implementation of a Human Rights Committee to Facilitate a Participant-Centered Approach to Research
Rosmery Sicilia
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Silbert, Leah

Cedars-Sinai
70 - Measuring Compliance with Policy for Processing Planned Protocol Deviations
Leah Silbert
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Simmons, Shannon

Vanderbilt University Medical Center Human Research Protections Program
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Shannon Simmons
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Smith, Belinda

University of Kentucky
21 - Development of the K-12 Teacher and Support Staff Human Subjects Protection Training Course
Belinda Smith
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Smith, Carrie

Wake Forest University Health Sciences
42 - Single IRB Stakeholder Feedback: Evaluating the Use of the IRB Reliance Exchange
Carrie Smith
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Soleas, Eleftherios

Queen's University
96 - Needs and Preferences of Research Ethics Board Members in the Development of a New TCPS 2 Training Program in Canada
Eleftherios Soleas
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Spedale, Melanie

Northwestern University
83 - Maintaining & Managing Satellite Facilities- How IACUCs Can Provide Necessary & Succinct Oversight with a Daily Activity Sheet
Melanie Spedale
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Spence, Cheryl

Novartis
81 - Compassion Fatigue and Compassion Satisfaction for Lab Animal Professionals: a program to bring Culture of Care to a global team
Cheryl Spence
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Spicer, Christina

Northwestern University
57 - Closing Time: Reconciling Lapsed Studies in an External IRB Portfolio
Christina Spicer
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Spiro, Avron

Department of Veterans Affairs Cooperative Studies Program Boston Coordinating Center
100 - Development and Implementation of a Human Rights Committee to Facilitate a Participant-Centered Approach to Research
Avron Spiro
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Spivey, Sheri

WCG IRB
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Sheri Spivey
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Sproston, Kylie

Bellberry Ltd
25 - Conceptualizing Human Research Ethics Committees as Regulatory Actors: Implications for Expectations and Practices
Kylie Sproston
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Stewart, Cameron

University of Sydney
25 - Conceptualizing Human Research Ethics Committees as Regulatory Actors: Implications for Expectations and Practices
Cameron Stewart
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Stockley, Denise

Queen's University
96 - Needs and Preferences of Research Ethics Board Members in the Development of a New TCPS 2 Training Program in Canada
Denise Stockley
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Stubbs, Susie

United States Army Criminal Investigation Division
63 - Post-Approval Compliance Monitoring in a Military Prison
Susie Stubbs
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Sullivan, Karlee

Scripps Research
87 - Optimizing Post-Approval Monitoring: Using SafetyCulture for Enhanced Compliance and Animal Welfare
Karlee Sullivan
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Suver, Christine

Sage Bionetworks
72 - A Landscape Survey of Generalist Data Repositories to Facilitate Researcher Selection and IRB Review
Christine Suver
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Tadeo, Monique

U.S. EPA
47 - Tracking non-Protocol Review-related HRPP activities
Monique Tadeo
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Tanner, Adrienne

University of California, Berkeley
37 - Navigating Ancillary Compliance Requirements During the IRB Review Process
Adrienne Tanner
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Mohammed bin Rashid Center for Special Education operated by the New England Center for Children
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Aida Tarifa-Rodriguez
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University of Alabama at Birmingham
41 - Implementing a Career Ladder for a Healthier Midsection
Lauren Tarpley McGibboney
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Tate, Wendy

Advarra
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Wendy Tate
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Tatman, Chariss

Univeristy of Utah
8 - Does a dedicated research language services team increase enrollment and retention in Spanish speaking participants?
Chariss Tatman
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Taylor, Holly

NIH
23 - The ENVISION Project: Creating a values-oriented platform for informed consent.
Holly Taylor
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Towsley, Nyssa

University of Nevada, Las Vegas
6 - What to Expect When You Don’t Know If You’re Expecting: Best Practices for Discussing Pregnancy Status and Testing with LGBTQIA+ Individuals
Nyssa Towsley
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45 - Revising the IRB Submission Form: Lessons Learned From the Design Process
Nyssa Towsley
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Intermountain Health
59 - Engaging IRB Chairs: Analysis of the Working Relationship of IRB Staff and Chairs prior to IRB Meetings
Melinda Tracy
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60 - Reimagining IRB Rosters: Reducing Reviewer Burden amid a Growing Research Program
Melinda Tracy
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Indiana University School of Medicine, Indiana CTSI
76 - Ethical and Procedural Interplay between Ongoing Research Programs and Ancillary Studies
Amy Trullinger
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Truong, Albert

Genentech
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Albert Truong
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Seattle Children's Research Institute
23 - The ENVISION Project: Creating a values-oriented platform for informed consent.
Jennifer Tsing
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Turnock, Stephen

NC3Rs
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Stephen Turnock
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MSKCC
91 - A one year review of enhancements to our Continuing Review Submission Process.
Michael Tuttle
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Washington University School of Medicine
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Amila Tutundzic
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66 - Addressing Barriers to Sustained Monitoring
Amila Tutundzic
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Morehouse School of Medicine
88 - Advancing Diversity in Clinical Research through the Clinical Research Coordinator Certificate (CRCC) Program
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Valentino, Emily

Memorial Sloan Kettering Cancer Center
44 - Respect for the Reader: Language Sensitivity in Informed Consent Forms
Emily Valentino
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Columbia University in the City of New York
58 - Evaluation of Virtual and In-person IRB Meetings During Calendar Year 2023 and 2024
Justin Vargas
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Novartis
81 - Compassion Fatigue and Compassion Satisfaction for Lab Animal Professionals: a program to bring Culture of Care to a global team
Georgianna Varrone
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Genentech
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Amy Vassel
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Velders, Jeanne

Washington University School of Medicine
66 - Addressing Barriers to Sustained Monitoring
Jeanne Velders
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77 - Is this Single IRB in Disguise?
Jeanne Velders
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U.S. Army DEVCOM Armaments Center
63 - Post-Approval Compliance Monitoring in a Military Prison
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Centers for Disease Control and Prevention (CDC)
95 - Effectiveness of a Virtual Training Program, 2023
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The University of Auckland
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Javier Virues-Ortega
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Wang, Yumeng

The Society of Medical Ethics of China Anti-Cancer Association
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Yumeng Wang
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Yumeng Wang
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The Mohammed bin Rashid Center for Special Education operated by The New England Center for Children
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Shannon Ward
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65 - A Survey of Researchers’ Experiences with Assent and Child Participants in Research
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Weiss, Daiana

Emory University
101 - Customized Risk-Based Post-Approval Monitoring Sessions to Improve Animal Welfare Related Compliance
Daiana Weiss
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Wilfond, Benjamin

Seattle Children's Research Institute
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Benjamin Wilfond
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Williams, Ashley

University of Virginia
79 - Effective IRB advising for undergraduate researchers: a multi-pronged approach
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Vail Health Hospital
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Sierra Willis
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Lakeland Regional Health
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Trudy Wittenberg
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Teachers College, Columbia University
32 - Successful Virtual IRB Meetings
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X
Xie, Jiale

Queen's University
96 - Needs and Preferences of Research Ethics Board Members in the Development of a New TCPS 2 Training Program in Canada
Jiale Xie
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Yakin, Syamil

Nationwide Children's Hospital
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Syamil Yakin
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Yakubu, Aminu

Center for Bioethics and Research, Ibadan, Oyo State, Nigeria
99 - Scoping Review of the Ethical Regulations for Alzheimer’s Disease and Alzheimer’s Disease Related Dementia Research in Africa
Aminu Yakubu
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Yan, Zhao

The Society of Medical Ethics of China Anti-Cancer Association
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Zhao Yan
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Zhao Yan
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Youngblood, Laura

Centers for Disease Control and Prevention (CDC)
95 - Effectiveness of a Virtual Training Program, 2023
Laura Youngblood
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Z
Zand, Rachel

University of Toronto
96 - Needs and Preferences of Research Ethics Board Members in the Development of a New TCPS 2 Training Program in Canada
Rachel Zand
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Zhang, Yumei

Peking University
11 - Patients attitudes towards the sharing of electronic health records for medical research
Yumei Zhang
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Zhao, Liyan

Peking University
11 - Patients attitudes towards the sharing of electronic health records for medical research
Liyan Zhao
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Zhou, Ming

China Anti-Cancer Association
33 - Exploration of the Mutual Recognition Mechanism for Ethical Review in Chinese Oncology Clinical Trials
Ming Zhou
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Ming Zhou
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Znidarsic, Maria

Cystic Fibrosis Foundation
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Maria Znidarsic
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Zolondek, Corey

University of Michigan
16 - Participant Payments and Undue Influence
Corey Zolondek
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17 - Third-Party Vendor Policy Awareness Program
Corey Zolondek
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