'Informed consent document' diaporamas de présentation

CLINICAL TRIALS

CLINICAL TRIALS. AUTHOR Dr .A. K. AVASARALA MBBS,M.D. PROFESSOR &HEAD DEPT OF COMMUNITY MEDICINE & EPIDEMIOLOGY PRATHIMA INSTITUTE OF MEDICAL SCIENCES, KARIMNAGAR,A.P.. INDIA : +91505417 avasarala@yahoo.com. LEARNING OBJECTIVES.

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Subpart A Subcommittee (SAS)

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Basics of Informed Consent (Part 1)

Basics of Informed Consent (Part 1). Paula Bistak, DMH, RN, MS, CIP, CHRC Executive Director, HSPP Donna Hoagland, LPN, BS, CIP, CCRC, CHRC IRB Director, New Brunswick/Piscataway and Stratford/Camden Carlotta Rodriguez, BS, CIP, CHRC IRB Director, Newark Campus IRB

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Good Clinical Practice

Good Clinical Practice. A Review for OCRA US RAC Study Group September 2005 Ginger Clasby, MS Promedica International gclasby@promedica-intl.com 714-799-1617 x 25. GCP What It Is.

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PUI Compliance

PUI Compliance. Assessment and Design of a Realistic Compliance Program. Taking Stock of the Regulations. Determine campus stakeholders Assess acceptance of readiness for change Assess operational capability Cultivate champions for communication and education of different campus groups

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Understanding Informed Consent in Outpatient Mental Health

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Genomics and Personalized Healthcare Lecture 2

Genomics and Personalized Healthcare Lecture 2. Bailee Ludwig Quality Management. Outline. The Human Genome Project Quality & Safety Genomic Ethics Genetic Law Risk Perception and Health Behavior Scenarios. The Human Genome Project.

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IRB BASICS: Ethics and Human Subject Protections

IRB BASICS: Ethics and Human Subject Protections. The Committees on Human Research University of Vermont & Fletcher Allen Health Care. IRB Function.

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Informed Consent

Informed Consent. Ghaiath M. A. Hussein MBBS, MHSc. (Bioethics) Research Ethics Workshop, Medani (Dec., 08). INFORMED CONSENT.

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Method Section

Method Section. Describing the procedure. Steps in this tutorial. 1) State the goals of this tutorial 2) What is a method section 3) What is in a method section 4) What is the procedure part of a method section 5) What goes in the procedure section

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FERPA and IRB: Implications for Testing Centers

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HHS Reporting Requirements and Adverse Events

Michael A. Carome, M.D. Director, Division of Compliance Oversight Office for Human Research Protections. HHS Reporting Requirements and Adverse Events. Title 45 Code of Federal Regulations Part 46 Protection of Human Subjects (Last revised June 18, 1991). Educational Objectives.

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Unlocking the Mystery of General Information Reporting

Unlocking the Mystery of General Information Reporting. Research Compliance Administration Training Presentation Wednesday, June 6, 2007 Presenter: Heather Kemp 278-7812 hkemp@iupui.edu. Prompt Reporting Form Section I.

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Research Ethics

Research Ethics. PPAL 6200-3.0 7-8 February, 2012. Introduction. Why? Regulatory Framework Administration of the Framework here at York Practical Advice. Why? The University Setting. Academic Freedom comes with Social Responsibility

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Results of the AAHRPP Visit

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IRB Review Process at IRB-HSBS

IRB Review Process at IRB-HSBS. IRB Health Sciences & Behavioral Sciences University of Michigan 2009-2010. Goals of this Audiocast. Describe possible IRB review paths Outline the general process of IRB review at IRB-HSBS Implications of timing of IRB submissions

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Consenting Withdrawn Subjects for Follow-Up Information

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Managing Boundaries

Managing Boundaries. Complete survey on page 283 Divide into Groups - Discuss the following: If a client could no longer afford to pay you for services, would you be willing to enter into a bartering agreement? What other alternatives would you utilize?

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