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IRB Application Process Research Ethics & Compliance

WEBThe IRB application is an online questionnaire/form that any member of the study team can initiate within U-M's eResearch Regulatory Management (eRRM) system. It's designed …

Actived: 1 days ago

URL: https://research-compliance.umich.edu/irb-application-process

IRB-HSBS Education Research Ethics & Compliance

WEBFor scheduling or questions, contact: IRB Health Sciences and Behavioral Sciences. Phone: (734) 936-0933. [email protected]. Lists the training and educational …

Category:  Health Go Health

IRB Review Process Research Ethics & Compliance

WEBIRB-HSBS Turnaround Times. "Turnaround" is the estimated time it takes to complete the IRB review and determination process. Full-board: 4 - 8 weeks. Expedited: 2 - 4 weeks. …

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Research Ethics & Compliance University of Michigan

WEBOur Campus Partners. Effective research compliance relies on cooperative oversight and action from multiple units. UMOR works with the schools and colleges and other U-M …

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Research Safety Research Ethics & Compliance

WEBFor more information about U-M research safety programs or for policy matters, call 734-936-3934 or send e-mail to [email protected]. For more information …

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PEERRS: Human Subjects Research Protections Course Details

WEBThe PEERRS Human Subjects Research Protections (HSP) course defines human subjects research, identifies the federal regulations that govern the research activity, explains …

Category:  Course Go Health

Human Subjects Protections Glossary Research Ethics

WEB"Human Subjects Protections" is a collective term for the federal, state, and university policies, procedures, and ethical considerations that protect the rights and welfare of …

Category:  Health Go Health

Routine fMRI Study Guidelines Research Ethics & Compliance

WEBRoutine fMRI Study Criteria. In order for an fMRI study to be eligible for IRB-HSBS review, the following criteria must be satisfied: The Principal Investigator (PI) …

Category:  Health Go Health

Human Research Protection Program (HRPP)

WEBFor UMHS Clinical Engineering services or consultation regarding the use (e.g., selection, safety, maintenance) of investigational devices in human subjects research, call 734-615 …

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IRB Health Sciences and Behavioral Sciences (HSBS)

WEBThe Health Sciences and Behavioral Sciences Institutional Review Board (IRB-HSBS) is responsible for protecting the rights and welfare of human participants in research …

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International Human Subject Research Resources

WEBThe external informational resources linked below address important areas for the development, approval, training for and conduct of international human subjects …

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Institutional Review Board

WEBIRB Health Sciences and Behavioral Sciences Standard Operating Procedures May 2020 1 PART 1 – INTRODUCTION, PURPOSE, AND ETHICAL PRINCIPLES I. The Human …

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International Human Subjects Research Risks

WEBInternational research risks extend beyond the boundaries of the university’s research oversight infrastructure. Mitigation must rely on thoughtful, informed judgments or …

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Guidance: Protecting Participant Privacy and Maintaining

WEBU-M HRPP Guidance: Protecting Participant Privacy and Maintaining Confidentiality of Data U-M Human Research Protections Program Updated: November 20192

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International Ethical Guidelines for Biomedical Research Involving

WEBThe Council for International Organizations of Mecial Sciences (CIOMS) guidelines (2016) reflect the conditions and the needs of biomedical research …

Category:  Medical Go Health

IRB-HSBS General Informed Consent Template Research Ethics

WEBDescription: (Word) Blank template with 2018 revised Common Rule key information and other required informed consent elements represented as section …

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Collaborative Research: IRB-HSBS sIRB Process

WEBThe Common Rule (45 CFR 46.114) requires that a single IRB-of-Record (sIRB) be designated to review and ongoing oversight of federally sponsored non …

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eResearch NextGen: Human Research Application

WEBeResearch NextGen uses an iterative design and review process with multiple working groups that focus on a regulatory requirement, application type or data component, or …

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