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OHRP: Human Research Protection Foundational Training | CITI Program OHRP: Human Research Protection Foundational Training Provides foundational training on human research protection. View this course at CITI Program.

The new course, "OHRP: Human Research Protection Foundational Training," provides foundational training on human research protection. You can now add this course to your organization's subscription.
https://post.citiprogram.org/4nm2vv5
#OHRP #HumanResearchProtection #CommonRule

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Webinars | CITI Program CITI Program offers webinars that reflect current topics important to our subscribing organizations and independent learners.

The new OHRP webinars explore key topics like the Common Rule, IRB review types, informed consent, and exemption categories. You can now add these webinars to your organization's subscription with our All Access Webinar Package.
post.citiprogram.org/4kFy9Sw
#OHRP #CommonRule #IRB #BelmontReport

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Considerations for Reviewing Human Subjects Research | CITI Program Considerations for Reviewing Human Subjects Research Covers various considerations for reviewing human subjects research, including subject selection, risk minimization, balancing risks and benefits,…

The new course, "Considerations for Reviewing Human Subjects Research," covers various considerations for reviewing human subjects research. You can now add this course to your organization's subscription as part of our Human Subjects Research series.
post.citiprogram.org/43k2qR6
#HSR #OHRP

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PRIM&R federal public policy briefing happening now — join in for discussions as to how recent changes are affecting research and the regulatory environment. Take action and contact your Congress members! primr.org/take-action/

#researchethics #research #OHRP #IRB

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We need to be asking if the HHS Office of Human Research Participants will be deleted. OHRP manages the ethical regulations for research and academics from ethical malfeasance on human beings in clinical trials. It regulates academic and institutional review boards (IRBs) who authorize trials. #OHRP

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