Ethics Rounds: Disagreements Between Clinicians and Researchers Over Proper Treatment: How Should They Be Resolved?
For more information go to http://www.cc.nih.gov/about/news/grcurrent.htmlAir date: 4/6/2016 12:00:00 PM (Source: Videocast - All Events)
Source: Videocast - All Events - March 18, 2016 Category: Journals (General) Tags: Upcoming Events Source Type: video
Wertheimer Remembrance: The challenge of shared decision making between physicians and patients
In Remembrance of Alan Wertheimer, PhD, the CC Department of Bioethics Presents the First Annual Widening the Lens Lecture
Alan Wertheimer's contributions to bioethics were far reaching and invaluable. After a very successful career in Political Science at the University of Vermont, Alan embraced bioethics with intellectual curiosity and acumen, often challenging prevailing views and urging broader thinking. He practiced a fruitful method - Widening the Lens (reflected in the title of this lecture and the subtitle of his last book), challenging all of us to consider why the norms and principles that guide our thinking abo...
Source: Videocast - All Events - March 7, 2016 Category: Journals (General) Tags: Upcoming Events Source Type: video
Reproducible Research: Many Dimensions and Shared Responsibilities
Biomedical researchers have an ethical responsibility to ensure the reproducibility and integrity of their work, so that precious research resources are not wasted and, most importantly, flawed or misleading results do not make their way to clinical studies where the faulty evidence could adversely affect study participants. Many factors have been suggested as contributors to irreproducible biomedical research, including poor study design, analytic instability of measurement methods, sloppy data handling, inappropriate and misleading statistical analysis methods, improper reporting or interpretation of results, and, on rar...
Source: Videocast - All Events - March 2, 2016 Category: Journals (General) Tags: Upcoming Events Source Type: video
Ethical and Regulatory Issues of Pragmatic Clinical Trails Workshop
The Workshop will focus on unique ethical and regulatory issues pertaining to pragmatic clinical trials that have been identified in the NIH Common Fund Collaboratory ProgramAir date: 5/10/2016 8:00:00 AM (Source: Videocast - All Events)
Source: Videocast - All Events - February 23, 2016 Category: Journals (General) Tags: Upcoming Events Source Type: video
CC Grand Rounds: Ethics Rounds: What is the Appropriate Design for Research on Suicide?
Presented by: Discussant: Donald Rosenstein, MD, Director, Comprehensive Cancer Support Program and Professor and Vice Chair, Division of Hospital Psychiatry, University of North Carolina at Chapel Hill and Case Presenter: Elizabeth Ballard, MD, Research Fellow, ECategory: Clinical Center Grand RoundsAired date: 02/03/2016 (Source: Videocast - All Events)
Source: Videocast - All Events - February 4, 2016 Category: Journals (General) Tags: Past Events Source Type: video
CC Grand Rounds: Ethics Rounds: What is the Appropriate Design for Research on Suicide?
For more information go to http://www.cc.nih.gov/about/news/grcurrent.htmlAir date: 2/3/2016 12:00:00 PM (Source: Videocast - All Events)
Source: Videocast - All Events - January 20, 2016 Category: Journals (General) Tags: Upcoming Events Source Type: video
Introduction to the Principles and Practice of Clinical Research (IPPCR) 2016: Ethical Principles in Clinical Research
Presented by: Christine Grady, R.N., Ph.D., NIHCategory: IPPCRAired date: 01/04/2016 (Source: Videocast - All Events)
Source: Videocast - All Events - January 6, 2016 Category: Journals (General) Tags: Past Events Source Type: video
Ethics Rounds: Is It Ethical to Conduct Research on Previous Obtained Cell Lines Without Donors' Consent
Presented by: Eric Juengst, PhD, Professor, Department of Genetics and Director, Center for Bioethics, University of North Carolina, Chapel Hill and Eugene Kane, MPH, Public Health Advisor, Office of Clinical Research, NIMH, NIHCategory: Clinical Center Grand RoundsAired date: 12/02/2015 (Source: Videocast - All Events)
Source: Videocast - All Events - December 2, 2015 Category: Journals (General) Tags: Past Events Source Type: video
Ethics Rounds: Is It Ethical to Conduct Research on Previous Obtained Cell Lines Without Donors' Consent
For more information go to http://www.cc.nih.gov/about/news/grcurrent.html
Air date: 12/2/2015 12:00:00 PM (Source: Videocast - All Events)
Source: Videocast - All Events - November 24, 2015 Category: Journals (General) Tags: Upcoming Events Source Type: video
The Ethics of Challenge Studies; Ethics of Research with Pregnant Women; Pragmatic Trials Case Discussion
DiscussionPresented by: Seema Shah, JD; Maggie Little, PhD; Scott Kim, MD PhDCategory: BioethicsAired date: 11/18/2015 (Source: Videocast - All Events)
Source: Videocast - All Events - November 19, 2015 Category: Journals (General) Tags: Past Events Source Type: video
Introduction to the Principles and Practice of Clinical Research (IPPCR) 2015: Ethical Principles in Clinical Research
The Introduction to the Principles and Practice of Clinical Research (IPPCR) is a course to train participants on how to effectively conduct clinical research. The course focuses on the spectrum of clinical research and the research process by highlighting epidemiologic methods, study design, protocol preparation, patient monitoring, quality assurance, and Food and Drug Administration (FDA) issues. For more information go to http://clinicalcenter.nih.gov/training/training/ippcr1.htmlAir date: 1/4/2016 5:00:00 PM (Source: Videocast - All Events)
Source: Videocast - All Events - November 16, 2015 Category: Journals (General) Tags: Upcoming Events Source Type: video
Ethics of Research with Children, Ethics of Randomized Trials, and mock IRB
Presented by: Robert “Skip” Nelson, MD, FDA; Robert Truog, MD, Harvard Medical SchoolCategory: BioethicsAired date: 11/04/2015 (Source: Videocast - All Events)
Source: Videocast - All Events - November 5, 2015 Category: Journals (General) Tags: Past Events Source Type: video
Clinical Trial Designs for Emerging Infectious Diseases (Day 2)
The Ebola Virus Disease (EVD) epidemic has highlighted the importance of being able to rapidly evaluate investigational products during a public health emergency, including in resource limited settings. It is generally agreed that access to early investigational interventions that have not yet been well characterized should be provided in a setting that allows for the reliable assessment of benefits and harms. Ascertaining the safety and efficacy of an investigational product is an important step that is necessary to protect and promote the public health now and in the future. A critical aspect of the response effort is t...
Source: Videocast - All Events - November 5, 2015 Category: Journals (General) Tags: Upcoming Events Source Type: video
Clinical Trial Designs for Emerging Infectious Diseases - Breakout Session (Day 2)
The Ebola Virus Disease (EVD) epidemic has highlighted the importance of being able to rapidly evaluate investigational products during a public health emergency, including in resource limited settings. It is generally agreed that access to early investigational interventions that have not yet been well characterized should be provided in a setting that allows for the reliable assessment of benefits and harms. Ascertaining the safety and efficacy of an investigational product is an important step that is necessary to protect and promote the public health now and in the future. A critical aspect of the response effort is t...
Source: Videocast - All Events - November 5, 2015 Category: Journals (General) Tags: Upcoming Events Source Type: video
Clinical Trial Designs for Emerging Infectious Diseases (Day 1)
The Ebola Virus Disease (EVD) epidemic has highlighted the importance of being able to rapidly evaluate investigational products during a public health emergency, including in resource limited settings. It is generally agreed that access to early investigational interventions that have not yet been well characterized should be provided in a setting that allows for the reliable assessment of benefits and harms. Ascertaining the safety and efficacy of an investigational product is an important step that is necessary to protect and promote the public health now and in the future. A critical aspect of the response effort is t...
Source: Videocast - All Events - November 4, 2015 Category: Journals (General) Tags: Upcoming Events Source Type: video
