Ohrpp.research.ucla.edu

Conducting Risk-Benefit Assessments and Determining Level of …

WEBConducting Risk-Benefit Assessments. Role of the Investigator: When designing research studies, investigators are responsible for conducting an initial risk …

Actived: 8 days ago

URL: https://ohrpp.research.ucla.edu/assessing-risks/

What Type of Study Does Each of the Five IRBs Review

WEBDistinctions between biomedical and social behavioral research Biomedical research. Biomedical research refers to the study of specific diseases and conditions …

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Getting Started with an IRB Application UCLA Office of the …

WEBThe UCLA Office for the Human Research Protection Program (OHRPP) is the office that supports the 5 UCLA IRBs. Each of the five IRBs specialize in certain …

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Information For Research Participants UCLA Office of the Human

WEBInformation For Research Participants. UCLA is committed to protecting the rights, safety, and welfare of people who volunteer for research. Volunteers are also …

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National Cancer Institute Central IRB (NCI CIRB)

WEBThe Central Institutional Review Board (CIRB) Initiative is sponsored by the National Cancer Institute (NCI) in consultation with the Department of Health and …

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Quality Improvement Unit (QIU) UCLA Office of the Human …

WEBThe primary purpose of the Quality Improvement Unit (QIU) is to provide post-approval monitoring and internal oversight, education and training to research …

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SMART IRB UCLA Office of the Human Research Protection …

WEBSMART IRB is funded by the National Center for Advancing Translational Sciences (NCATS) and intended to serve as a roadmap for institutions to implement The National …

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Education and Training UCLA Office of the Human Research …

WEBThe Education and Training Unit within UCLA’s Office of the Human Research Protection Program provides training in the critical area of the protection of …

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Policies and Guidance UCLA Office of the Human Research …

WEB1. Authority and Overview of the Human Research Protection Program. UCLA Policy 991: Protection of Human Subjects in Research. Mission and Goals of OHRPP. …

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Human Subjects Protection Certification via CITI UCLA Office of …

WEBResources. NEW: Create a New CITI Program Account via UCLA SSO NEW: Link an Existing CITI Program Account via UCLA SSO Additional FAQs. For …

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About UCLA IRBs UCLA Office of the Human Research Protection …

WEBThe function of the IRBs is to ensure adherence to all federal, state, local, and institutional regulations concerning the protection of human subjects in research. …

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HIPAA Frequently Asked Questions UCLA Office of the Human …

WEBProtected or personal health information (PHI) is any information in the medical record or designated record set that can be used to identify an individual and that was created, …

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Contact Us UCLA Office of the Human Research Protection Program

WEBOHRPP. Telephone: (310) 825-5344 Email: [email protected] North & South General Institutional Review Boards (GIRB) Email: [email protected] …

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IRB Meeting Calendars UCLA Office of the Human Research …

WEBChair: Allan Pantuck, MD. IRB Administrator: Rebecca Stella (310) 794-9287. Medical Institutional Review Board 3 (MIRB3) Reviews neuroscience, neurology, …

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HIPAA Research Guidelines and Information UCLA Office of the …

WEBThe Health Insurance Portability and Accountability Act of 1996 (HIPAA) contains provisions to protect the confidentiality and security of personally-identifiable …

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Research Participant Bill of Rights/Experimental Subjects Bill of

WEBCalifornia law, requires that any individual (or Legally Authorized Representative) asked to participate in a research study defined as a "medical …

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The UCLA-RAND Memorandum Of Understanding (UCLA-RAND …

WEBThis MOU is a reciprocal agreement for research that falls within the scope of the UCLA-RAND Memorandum of Understanding (MOU) for Health Services Research.As the July …

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