Human Research Protections (HRP) is a comprehensive program that affords protections for all human research participants and is under the direct leadership of the Vice President and Chief Accountability Officer. This website provides up-to-date information related to conducting research with human participants.
Questions??? Ask the Chair and HRPO Staff!
This is an opportunity for the research community to speak directly to the IRB Chair and a member of the HRPO/IRB staff!!
2nd Monday of every month from 12n to 1pm.
First session: This Monday, October 14, 2024
Link:
(no RSVP required)
For Researchers: This resource helps investigators design, write, and organize research protocols; maintain compliance with policies and regulations; create and submit IRB applications via CICERO.
Institutional Review Board (IRB): Information about the board and the executive members and their role in approving, monitoring, and reviewing biomedical and behavioral research involving humans.
HRP Office: Information regarding its role in coordinating the Human Research Protections Program and providing support for the 海角官方首页 Institutional Review Board (IRB). Contact information and informatics regarding submission processing times.
For Research Participants: This section assists former, current, or prospective human research participants in obtaining information or offering input regarding research and clinical trials.
The IO is responsible for ensuring that the Human Research Protection Program (HRPP) functions effectively and that the institution provides the resources and support necessary to comply with all requirements applicable to research involving human subjects. Dr. Buskirk's IO Appointment Letter
The main focus here is to provide information, resources, and instructions for completing the review process through the IRB. While the IRB is a key player in the HRP program, there are many other components within 海角官方首页 critically involved in protecting human participants. Click here to learn more.
The Association for the Accreditation of Human Research Protection Programs, Inc. (AAHRPP) is an independent, non-profit accrediting body, AAHRPP uses a voluntary, peer-driven, educational model to ensure that HRPPs meet rigorous standards for quality and protection.
SMART IRB is a platform designed to ease common challenges associated with initiating multisite research and to provide a roadmap for institutions to implement the (effective date: January 25, 2018).
(Click to read all Past Announcements)
TO: 海角官方首页 Research Community:
A virtual town hall will be held for the 海角官方首页 research community to provide feedback on the goals of the 海角官方首页 Research Compliance strategic plan related to human, animal and laboratory research. Attendees may pose questions or comments personally or anonymously. This listening opportunity is designed for your voice to be heard!
Dr. Robert Rosenthal, Assistant Vice Provost Research Compliance and Dr. Julie Doherty, Assistant Vice President, Research Compliance, will be there to facilitate. We are looking forward to your participation !!
Link to recording:
Date: December 3, 2024
STRATEGIC GOAL 1: An efficient and effective research compliance program of the highest standards
STRATEGIC GOAL 2: Comprehensive educational opportunities for all
STRATEGIC GOAL 3: An inclusive and engaged research community
STRATEGIC GOAL 4: Innovative research enterprise
STRATEGIC GOAL 5: Ethical and compliant global research engagement
STRATEGIC GOAL 6: Security and Integrity of Research Data
Please join us!!
University of Maryland Baltimore
Human Research Protections Program
Virtual Grand Rounds:
Single IRBs: What Needs to be Reported to 海角官方首页 When Relying on an External IRB
Presenter: Julie Doherty, DM, MSN, RN, CIP, CCEP
Assistant Vice President, Research Compliance
October 30, 2024
1pm to 2pm
Recording Link:
Slides: Relying IRB--What Needs to be Reported RNI Oct. 30, 2024
Please join us!!
University of Maryland Baltimore
Human Research Protections Program
Virtual Grand Rounds
After IRB approval--What Needs to be Reported to the 海角官方首页 IRB?
(A Review of 海角官方首页 IRB HRPP Reportable New Information Submission requirements)
Presenter: Julie Doherty, DM, MSN, RN, CIP, CCEP
Assistant Vice President, Research Compliance
October 10, 2024
1pm to 2pm
Recording Link:
Slides: Recorded Webinar Slides - Oct 10th, 2024 Grand Rounds
Please join us!
5/30/2024 Seminar 12pm-1pm Virtual (Zoom)- Registration Required
Presentation: PI and Study Staff Considerations for QA/Monitoring
Presenter:
Jill Kessler MS, MSL, CCRP
Senior Research Monitor
Johns Hopkins University
Learning Objectives:
Recording Link:
Slides: Recorded Webinar Slides - May 30th, 2024 GR and SOCRA
Regards,
Casey Jackson, MS, CCRP (she/they)
Director, Research Quality Improvement and Compliance
Baltimore SOCRA Chapter Chair
SOCRA National Board Director
Please join us!!
海角官方首页 Human Research Protections Program Virtual Grand Rounds
海角官方首页 Research Compliance Coordinating Council Survey: Focus on the 海角官方首页 IRB: Survey Results and Plans for Improvement
May 29, 2024 2pm-3pm
In the early Fall 2023, a survey was conducted that included a request for feedback on the 海角官方首页 Institutional Review Board. This session will provide summary information on IRB survey feedback along with IRB plans for improvement in processes and procedures. Q&A session will be included.
Recording Link:
Robert Rosenthal, MD, Assistant Provost, Research Compliance
Julie Doherty, DM, MSN, CIP, CCEP, Assistant Vice President, Research Compliance
Jon Mark Hirshon, MD, PhD, 海角官方首页 Institutional Review Board Chair
Jan Martinez, MS, CIP, CLSSGB, 海角官方首页 Institutional Review Board Manager
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The University of Maryland, Baltimore is the founding campus of the University System of Maryland.
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