PPT-Informed Consent Allison Blodgett, PhD, CIP

Director of IRB Operations UMass Medical School Tuskegee Study This study was initiated in the 1930s as an examination of the natural history of untreated syphilis it continued until 1972 400 black men with syphilis participated. KSV NIMA Langmuir and Langmuir-Blodgett Deposition Troughs (KSV NIMA L & LB Troughs) are used for the fabrication and characterisation of single molecule thick �lms and o�er the An IRB . Infoshort. , June 2013. Informed Consent: Basis. The federally mandated requirements for informed consent are grounded in the Belmont Report.. . Respect for Persons:. “Respect for persons incorporates at least two ethical convictions: first, that individuals should be treated as autonomous agents, and second, that persons with diminished autonomy are entitled to protection. The principle of respect for persons thus divides into two separate moral requirements: the requirement to acknowledge autonomy and the requirement to protect those with diminished autonomy. Christine Hasha. Matt Mereness. April 2015. At the end of this presentation you will be able to:. Explain why the electricity industry is under federal regulation for physical and cyber protection. Describe some of the physical and cyber risks to the electric grid. Jeri R. . Barney. , JD, . MS . . Michele . Antisdel, . MBA/CCRP. HRPP Compliance Manager IRB Regulatory Analyst. Human Research Protection Program (HRPP). May 16, 2013. Discussion. Consent Process. Consent and HIV Cure Research. HIV Cure Research Training Curriculum. Informed Consent Module by:. . Gail E. Henderson, UNC School of Medicine. Professor, Department of Social Medicine. Janet G. Lenz, Ph.D.. Gary W. Peterson, Ph.D. .. Robert C. Reardon, Ph.D.. James P. Sampson, Jr., Ph.D.. Florida State University. Denise E. Saunders, Ph.D.. Private Practice. National Career . Development Association, June . Phronesis. in the Classroom. Experimenting on your students ethically via an example of experimenting on Chinese students’ written coherence. Neil.Allison@glasgow.ac.uk. Phronesis. – practical wisdom. and Refusal of Treatment. The notion of informed consent is a recent one. . Prior to the 1950’s, there was no firm ground in which a commitment to informed consent could be grounded. . It is important that we work to understand exactly what it means to make an informed decision, so that we can be certain that our patients are able to act autonomously. . Assistant Director of Compliance. Office of Human Research (OHR). patrick.herbison@jefferson.edu. These slides contain summaries of regulations (mainly 45 CRF 46) and OHR Policies. Please follow the full regulations and policies.. Jeri R. . Barney. , JD, . MS . . Michele . Antisdel, . MBA/CCRP. HRPP Compliance Manager IRB Regulatory Analyst. Human Research Protection Program (HRPP). May 16, 2013. Discussion. Consent Process. Content, Documentation, Broad Consent, and Posting of Informed Consent Forms. 1. Overview. Introduction. Major changes to informed consent content and process. Broad consent. Waiver of Alteration of Informed Consent. version: February 2021 . Example. 2. Someone you don’t know hands you a cup of tea.. Questions that may come to mind:. Who made this tea?. What is in this tea?. Why was I given this tea?. Prospective participants may have similar questions when you ask them to participate in research.. Waiver of Consent, Alteration of Consent, and Waiver to Document Consent . Definitions. Waiver of consent – the IRB waives all consent requirements (process, document, signature). Alteration – the IRB waives some or alters some of the elements of informed consent (document, signature). Webinar. Introduction and Framework. Pooja Khatri, MD MSc. Welcome. Local IRB and HRPP officials. PIs and Coordinators. RCC. Satellite. Trial. Why now?. COVID-19 increases urgency. Improves ICF process regardless.