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University of Pennsylvania, School of Medicine

Disclaimer Please cite the appropriate authors/contacts when using or adapting these materials.
Acknowledgment Emma A. Meagher, M.D.
Associate Professor of Medicine and Pharmacology
Coordinator, POR & MTR Programs
University of Pennsylvania
Contacts Marti Dandridge, Coordinator, Masters of Science in Translational Research, (MTR) Program
Format PowerPoint?
URL Download
Materials Provided PPT (25 Slides)
Title Biomedical Ethics Research Overview
Topics Description This is a comprehensive well organized presentation that covers scientific integrity, and past egregious conduct that has happened in both clinical trials and basic research. The important regulatory oversight bodies and rules that have developed to address past ethical breaches and insure scientific integrity now and in the future, knowing it is vital to educate upcoming researchers about the importance of ethics in scientific research. Other areas addressed are data management, authorship, conflicts of interest, peer review, and rounded out with misconduct. In addition, this presentation has 3 case studies (Data Management, Peer Review, and Confidentiality).
Keywords Adverse Events (AE); Animal Welfare; Association for Assessment of Laboratory Animal Care (AALAC); Authorship; Brigham; Conflicts of Interest; Corporate Payments; Data Management; Data Sharing; Department of Health and Human Services (DHHS); Disclose Financial Conflicts; Fabrication; Falsification; Gene Therapy; Good Clinical Practice (GCP); Graduated Studies Authorship; Health Insurance Portability and Accountability Act (HIPAA); Human Subjects; Informed Consent; Institutional Animal Care and Use Committee (IACUC); Institutional Review Board (IRB) Process; Investigational Device Exemption (IDE); Investigational New Drug (IND); Mandated Bioethics Training; Mandated Confidentiality of Patient information; Mendel; Monitoring; National Institutes of Health (NIH); Nazi War Crimes; Objective; Office for Human Research Protections (OHRP); Office for Protection from Research Risks (OPRR); Office of Research Integrity (ORI); Order of Authors; Patient Rights; Plagiarism; Public Health Service (PHS); Qualifications for Authorship; Regulatory Oversight; Research Misconduct; Scientific Misconduct; Serious Adverse Events (SAE); Freedom of Information Act (FOIA); Sloan Kettering; Tuskegee Experiments; Vascular Endothelial Growth Factor (VEGF); Vulnerable Populations; Whistleblowers; Whitehead
See Also

Topic Data Acquisition Management Sharing and Ownership, Conflicts of Interest and Commitment, Human Subjects, Animal Welfare, Research Misconduct, Publication Practices and Responsible Authorship, Peer Review, Collaborative Science, Other
Topic attachments
I Attachment Action Size Date Who Comment
pptppt Biomedical_Research_Ethics_Overview-UofPennsylvania.ppt manage 214.0 K 10 Jun 2009 - 20:58 NancyHills PPT presentation (25 slides)
Topic revision: r4 - 30 Mar 2010 - 19:38:11 - MaryBanach
ResearchEthics.Biomedical_Ethics_Research_Overview moved from ResearchEthics.BiomedicalEthicsResearchOverview on 12 Jun 2009 - 19:12 by CTSpediaAdmin - put it back
 
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