'Consent process' presentation slideshows

HISTORY OF INFORMED CONSENT

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Part 2 of 3 part series: Informed consent: The Process

Part 2 of 3 part series: Informed consent: The Process. Wendy Lloyd BA, LPN , CIP,CCRP Regulatory Affairs and Compliance Specialist. Objectives. Identify consent process requirements Distinguish between IRB, PI/Designee consent process responsibilities

759 views • 52 slides

Research Involving Human Subjects

Research Involving Human Subjects. Institutional Review Board (IRB) Judette Haddad, PhD, CIP. History and Ethical principles. Nuremberg Code 1947 Declaration of Helsinki 1964 National Research Act 1974 Belmont Report 1979 Respect for person- Informed consent

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The Informed Consent Process: From Rules and Regulations to the Protective Value of Ethics

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Research involving cognitively impaired persons

Research involving cognitively impaired persons. Chin Jing Jih Adjunct Assoicate Professor, NUS Centre for Biomedical Ethics Programme Director, NHG Research Quality Assurance Deputy Co-Chair, NHG Research Ethics Committee. Outline. Definition of cognitive impairment

498 views • 32 slides

Inside the Research Process & Protocol

Inside the Research Process & Protocol. Inside the Research Process Process. The research process includes:. The idea, need, priority, question, interest, opportunity. Obtaining support. Conducting project activities. Interpreting results. Disseminating results.

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ICF Process

ICF Process. IRB Webinar 11/13/2014. Objectives. To recognize how to conduct an adequate informed consent process in adults and children To learn how to manage the process in special situations To identify things to avoid when documenting the process. Topics. Introduction

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NATIONAL ATAXIA REGISTRY

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Informed Consent and the Research Process

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Consent; Roles and Responsibilities

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Informed Consent: Process, Documentation, Alteration and Waivers

Informed Consent: Process, Documentation, Alteration and Waivers. Suzanne Sparrow. Objectives. Significance & History Regulations (DHHS/FDA) Elements of Consent Waiving/altering consent Waiving documentation of consent Process of consent

326 views • 18 slides

Post Approval Monitoring Program

Post Approval Monitoring Program. by Louisa Gay Post Approval Monitoring Officer. What is Post Approval Monitoring Why should we do this Who will be involved Logistics Questions. Discussion Areas.

338 views • 15 slides

Patient Satisfaction Survey Endoscopy Unit STHK

Patient Satisfaction Survey Endoscopy Unit STHK. Diane Conway February 2013. Demographics. British 97% Indian 3% European 1 %. Gender. Ethnicity. Methodology / patient group.

328 views • 14 slides

Phase O Trials: Ethical Considerations

Phase O Trials: Ethical Considerations. Holly Taylor, PhD, MPH Department of Health Policy and Management Bloomberg School of Public Health Berman Institute of Bioethics Johns Hopkins University. Summary. Subject Understanding Respect for Persons Empirical Evidence from Phase I

247 views • 13 slides

The Role of Patient Advocates in Research

4 th Annual Medical Research Summit April 22, 2004. The Role of Patient Advocates in Research. Deborah E . Collyar PAIR: Patient Advocates In Research InterSPORE Patient Advocate/Research Team (PART) Program. Why Advocates In Research?. Bridging the Research Gap

290 views • 12 slides

Good Clinical Practice GCP overview

Good Clinical Practice GCP overview. Research for Better Health Outcomes - Workshop March 9, 2011. Content. Historical perspective Origins of ICH / GCP Principles of GCP Informed consent. Historical Perspective. Nuremberg Code (1948) Kefauver-Harris Amendment (1962)

1.6k views • 11 slides

Overview of Findings from 2009-10

Overview of Findings from 2009-10. Students Instruments/scales IRBs and consent process Principal letter Parent Consent Student Assent. Water Resources: Preliminary Results. Student Demographics The fall simulations had a total of 506 consenting participants.

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