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CLINICAL TRIALS

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.

By kioko
(344 views)

FERPA and IRB: Implications for Testing Centers

FERPA and IRB: Implications for Testing Centers

FERPA and IRB: Implications for Testing Centers. Judith W. Grant, Ph.D.,CIP NCTA Conference San Antonio, Texas August 6, 2009. Welcome to San Antonio. It isn’t always this hot! Please come back in February!. FERPA. Family Educational Rights and Privacy Act

By matt
(170 views)

Managing Boundaries

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?

By Patman
(198 views)

HHS Reporting Requirements and Adverse Events

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.

By Gabriel
(138 views)

Method Section

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

By inez
(162 views)

Genomics and Personalized Healthcare Lecture 2

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.

By argyle
(123 views)

Unlocking the Mystery of General Information Reporting

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.

By lenore
(131 views)

IRB Review Process at IRB-HSBS

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

By meadow
(160 views)

Research Ethics

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

By elana
(103 views)

Results of the AAHRPP Visit

Results of the AAHRPP Visit

Results of the AAHRPP Visit. An IRB infoshort for IRB Members October 2013. Unanticipated Problems Involving Risks to Subjects or Others (UPIRSO) versus Serious Adverse Events (SAEs). GOALS. AAHRPP site-visit observation Definitions – UPIRSO and SAE

By miracle
(112 views)

PUI Compliance

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

By eamon
(153 views)

Consenting Withdrawn Subjects for Follow-Up Information

Consenting Withdrawn Subjects for Follow-Up Information

Consenting Withdrawn Subjects for Follow-Up Information. Anita Camic Team Leader Research Compliance Administration Tara Bateman Research Compliance Coordinator Research Compliance Administration. To Consent or Not to Consent: That’s the Question!.

By kare
(94 views)

Basics of Informed Consent (Part 1)

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

By lot
(81 views)

IRB BASICS: Ethics and Human Subject Protections

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.

By ziv
(76 views)

Informed Consent

Informed Consent

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

By hal
(193 views)

Today’s Agenda

Today’s Agenda

Today’s Agenda. Random variable review Overview of clicker experiment and informed consent Survey of attitudes toward statistics and clickers Comprehensive Assessment of Outcomes for a first course in Statistics (CAOS). Random Variable Review: The Qwizdom Years.

By eris
(81 views)

Subpart A Subcommittee (SAS)

Subpart A Subcommittee (SAS)

Subpart A Subcommittee (SAS). Elizabeth Bankert and Daniel Nelson Co-Chairs. Presentation to the Secretary’s Advisory Committee on Human Research Protections (SACHRP) July 16, 2008. Outline of Today’s Presentation. Subcommittee charge and membership Recommendations for consideration today

By irma-brennan
(96 views)

Understanding Informed Consent in Outpatient Mental Health

Understanding Informed Consent in Outpatient Mental Health

Understanding Informed Consent in Outpatient Mental Health. Presented by: Robert W. Marrs, MS, LMFT AAMFT Approved Supervisor. On Behalf of Wisconsin Association for Marriage and Family Therapy. Wisconsin Law – DHS 94.

By wayne-norman
(86 views)

Good Clinical Practice

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.

By cyrus-ramos
(239 views)

Today’s Agenda

Today’s Agenda

Today’s Agenda. Random variable review Overview of clicker experiment and informed consent Survey of attitudes toward statistics and clickers Comprehensive Assessment of Outcomes for a first course in Statistics (CAOS). Random Variable Review: The Qwizdom Years.

By awentia-jackson
(87 views)

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