citi completion report 4311916

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COLLABORATIVE INSTITUTIONAL TRAINING INITIATIVE (CITI) HUMAN SUBJECTS PROTECTION CURRICULUM COMPLETION REPORT Printed on 09/02/2014 LEARNER Hannah Johnson (ID: 4311916) 150 Ligon St apartment 902 clemson sc 29631 united states DEPARTMENT Medex PHONE 7046418782 EMAIL [email protected] INSTITUTION Greenville Health System EXPIRATION DATE 09/01/2016 BIOMEDICAL/CLINICAL RESEARCH : Includes studies that are FDA and Non-FDA Regulated COURSE/STAGE : Basic Course/1 PASSED ON : 09/02/2014 REFERENCE ID : 13880872 REQUIRED MODULES DATE COMPLETED Avoiding Group Harms - U.S. Research Perspectives 09/02/14 Recognizing and Reporting Unanticipated Problems Involving Risks to Subjects or Others in Biomedical Research 09/02/14 Humanitarian Use Devices (HUDs) 09/02/14 Belmont Report and CITI Course Introduction 09/02/14 History and Ethics of Human Subjects Research 09/02/14 Basic Institutional Review Board (IRB) Regulations and Review Process 09/02/14 Informed Consent 09/02/14 Social and Behavioral Research (SBR) for Biomedical Researchers 09/02/14 Records-Based Research 09/02/14 Genetic Research in Human Populations 09/02/14 Research With Protected Populations - Vulnerable Subjects: An Overview 09/02/14 Vulnerable Subjects - Research Involving Prisoners 09/02/14 Vulnerable Subjects - Research Involving Children 09/02/14 Vulnerable Subjects - Research Involving Pregnant Women, Human Fetuses, and Neonates 09/02/14 FDA-Regulated Research 09/02/14 Research and HIPAA Privacy Protections 09/02/14 Vulnerable Subjects - Research Involving Workers/Employees 09/02/14 Conflicts of Interest in Research Involving Human Subjects 09/02/14 Overview of U.S. FDA Regulations for Medical Devices 09/02/14 Informed Consent in Clinical Trials of Drugs, Biologics, and Devices 09/02/14 Audits and Inspections of Clinical Trials 09/02/14 For this Completion Report to be valid, the learner listed above must be affiliated with a CITI Program participating institution or be a paid Independent Learner. Falsified information and unauthorized use of the CITI Program course site is unethical, and may be considered research misconduct by your institution. Paul Braunschweiger Ph.D. Professor, University of Miami Director Office of Research Education CITI Program Course Coordinator

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  • COLLABORATIVE INSTITUTIONAL TRAINING INITIATIVE (CITI)HUMAN SUBJECTS PROTECTION CURRICULUM COMPLETION REPORT

    Printed on 09/02/2014

    LEARNER

    Hannah Johnson (ID: 4311916) 150 Ligon St apartment 902 clemson sc 29631 united states

    DEPARTMENT MedexPHONE 7046418782EMAIL [email protected] Greenville Health SystemEXPIRATION DATE 09/01/2016

    BIOMEDICAL/CLINICAL RESEARCH : Includes studies that are FDA and Non-FDA Regulated

    COURSE/STAGE: Basic Course/1PASSED ON: 09/02/2014REFERENCE ID: 13880872

    REQUIRED MODULES DATE COMPLETEDAvoiding Group Harms - U.S. Research Perspectives 09/02/14Recognizing and Reporting Unanticipated Problems Involving Risks to Subjects or Others in Biomedical Research 09/02/14Humanitarian Use Devices (HUDs) 09/02/14Belmont Report and CITI Course Introduction 09/02/14History and Ethics of Human Subjects Research 09/02/14Basic Institutional Review Board (IRB) Regulations and Review Process 09/02/14Informed Consent 09/02/14Social and Behavioral Research (SBR) for Biomedical Researchers 09/02/14Records-Based Research 09/02/14Genetic Research in Human Populations 09/02/14Research With Protected Populations - Vulnerable Subjects: An Overview 09/02/14Vulnerable Subjects - Research Involving Prisoners 09/02/14Vulnerable Subjects - Research Involving Children 09/02/14Vulnerable Subjects - Research Involving Pregnant Women, Human Fetuses, and Neonates 09/02/14FDA-Regulated Research 09/02/14Research and HIPAA Privacy Protections 09/02/14Vulnerable Subjects - Research Involving Workers/Employees 09/02/14Conflicts of Interest in Research Involving Human Subjects 09/02/14Overview of U.S. FDA Regulations for Medical Devices 09/02/14Informed Consent in Clinical Trials of Drugs, Biologics, and Devices 09/02/14Audits and Inspections of Clinical Trials 09/02/14

    For this Completion Report to be valid, the learner listed above must be affiliated with a CITI Program participating institution or be a paidIndependent Learner. Falsified information and unauthorized use of the CITI Program course site is unethical, and may be consideredresearch misconduct by your institution.

    Paul Braunschweiger Ph.D.Professor, University of MiamiDirector Office of Research EducationCITI Program Course Coordinator