'Continuing review' presentation slideshows

Continuing review - PowerPoint PPT Presentation


Welcome to IRBManager!

Welcome to IRBManager!

Welcome to IRBManager!. To access IRBManager , type the following address in your web browser: https://login.irbmanager.com/ Enter your username and password For “client”, enter “ uindy ”. Initial Access to IRBManager.

By adamdaniel
(338 views)

Kimberly Summers, PharmD Deputy ACOS for Research South Texas Veterans Health Care System

Kimberly Summers, PharmD Deputy ACOS for Research South Texas Veterans Health Care System

VA Research: IRB and R&D Approval Process From Initial Submission, Through the Informed Consent Process and Continuing Review, To Inactivation. Kimberly Summers, PharmD Deputy ACOS for Research South Texas Veterans Health Care System Research & Development Service. Overview.

By helki
(155 views)

Town Hall Q&A Session

Town Hall Q&A Session

Dial in: (415) 655-0060 Access Code: 812-008-474 Slides in “Handout” Tab. Town Hall Q&A Session. Hosted by ORPP&E; ORO P&E; and VHA Privacy. January 15, 2019. Presenters. Dial in: (415) 655-0060 Access Code: 812-008-474 Slides in “Handout” Tab. Overview of Session.

By brooke
(142 views)

Kimberly Summers, PharmD Deputy ACOS for Research South Texas Veterans Health Care System Research & Development Ser

Kimberly Summers, PharmD Deputy ACOS for Research South Texas Veterans Health Care System Research & Development Ser

VA Research: IRB and R&D Approval Process From Initial Submission, Through the Informed Consent Process and Continuing Review, To Inactivation. Kimberly Summers, PharmD Deputy ACOS for Research South Texas Veterans Health Care System Research & Development Service. Overview.

By moe
(175 views)

Wayne State University Detroit, MI

Wayne State University Detroit, MI

Wayne State University Detroit, MI . The Human Subjects’ Protection Regulations and You: What Everyone Should Know October 25, 2010 Elyse I. Summers, J.D. Director Division of Education and Development. Outline. History/Background Ethical Principles Overview of OHRP

By aure
(97 views)

Best practices for applying for human ethics approval Research Day August 31, 2006

Best practices for applying for human ethics approval Research Day August 31, 2006

Best practices for applying for human ethics approval Research Day August 31, 2006. Susan Blum, Ph.D. Manager, Ethics Office. Research Ethics. Nuremberg Code (1947) Declaration of Helsinki (1964) Belmont Report (1979) Universal Declaration on Bioethics

By malaya
(0 views)

Subpart A Subcommittee (SAS)

Subpart A Subcommittee (SAS)

Subpart A Subcommittee (SAS). Felix Gyi and Daniel Nelson Co-Chairs. Presentation to the Secretary’s Advisory Committee on Human Research Protections (SACHRP) October 29, 2007. Outline of Today’s Presentation. Subcommittee charge and membership Update on prior recommendations

By genevieve
(166 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)

Ethical Factors in the Recruitment and Retention of Research Participants

Ethical Factors in the Recruitment and Retention of Research Participants

Ethical Factors in the Recruitment and Retention of Research Participants. Frederick W. Luthardt, MA, MA Research Participant Advocate, ICTR Bayview CRU Compliance Specialist, JHM OHSR. Introduction …or, preaching to the choir. The real-world question: “Isn’t following the rules enough?

By kylene
(212 views)

IRB’s Top Ten*

IRB’s Top Ten*

IRB’s Top Ten*. What Every Investigator (and his/her research staff) Should Know about Conducting Human Research Activities. Investigator Responsibilities. * Based on David Lettermen’s Top Ten . PI Responsibility #1.

By venus
(135 views)

Workshop on the Protection of Human Subjects in Research Texas Christian University

Workshop on the Protection of Human Subjects in Research Texas Christian University

Workshop on the Protection of Human Subjects in Research Texas Christian University August 24, 2012 Brian Gladue, PhD, CIP Director, Office the Protection of Human Subjects (OPHS)\ Chair, Institutional Review Board (IRB). Human Research Subject Protection.

By knoton
(179 views)

Continuing Review

Continuing Review

Continuing Review. Presented by: Karen Jeans, PhD, CCRN, CIP Program Analyst, COACH. Objectives. Describe what is meant by “continuing review” Describe VA requirements for continuing review Calculate dates for continuing review expiration. What is Meant by Continuing Review?.

By nyx
(143 views)

Budgeting for Clinical Trials

Budgeting for Clinical Trials

Budgeting for Clinical Trials. Carolyn Strickland, RN, BSN, CCRC Research Billing Services Consultant Office of Contracts Management. Objectives. Review basics of a clinical trial budget Review “ PriceChecker ” on Starbrite Provide tips on the most common mistakes we see in OCM.

By azura
(229 views)

Responsible Conduct of Research Spring-1, 2014

Responsible Conduct of Research Spring-1, 2014

Responsible Conduct of Research Spring-1, 2014. Delia Y. Wolf, MD, JD, MSCI Associate Dean Regulatory Affairs and Research Compliance Harvard School of Public Health (HSPH) Email: dywolf@hsph.harvard.edu RCR Lecture-1, January 31 2014. Topics to be Covered.

By conan
(134 views)

Application for Initial Reviews

Application for Initial Reviews

Application for Initial Reviews. Human Subject Protection Office UConn Health Center Judy Gaffney, BA Monika Haugstetter, MHA, RN, MSN. http://resadm.uchc.edu/hspo/index.html.

By vevina
(116 views)

Presented by Sinclair Community College Institutional Review Board

Presented by Sinclair Community College Institutional Review Board

Research Ethics: The Protection of Human Subjects The Regulations and the Roles of the Researcher and the IRB. Presented by Sinclair Community College Institutional Review Board Adapted from materials provided by Frances Jeffries, Ph.D., Consultant, Bridgewater, MA.

By jamuna
(89 views)

2013 Certification Drive-in Conference

2013 Certification Drive-in Conference

2013 Certification Drive-in Conference Welcome to Georgia: Navigating the Approval Process and Supporting Georgia Educators. Dr. Hilda R. Tompkins Dr. Bobbi Ford November 12, 2013. Agenda. Who we are and what we do What’s on our website and where to find it Overview of PRS

By verda
(129 views)

The Institutional Review Board

The Institutional Review Board

The Institutional Review Board. Monica B. Spaulding, M.D. Chair-Health Sciences IRB Professor of Medicine. Outline. What is an IRB? Why does it exist What do we do IRB Reviews Full Expedited HIPAA Its impact on your research. What is an Institutional Review Board?.

By binta
(200 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) March 9-10, 2010. THIS VERSION REVISED AT SAS MEETING ON 6-2-10. Outline of Today’s Presentation.

By oriel
(102 views)

Site Visit Closing Meeting 30 October 2010

Site Visit Closing Meeting 30 October 2010

Site Visit Closing Meeting 30 October 2010. Presented by Dr Anoja Fernando Lead Surveyor UP Philippine General Hospital ERB Survey 28-30 October 2010. Objective and scope of the survey. Objective: To evaluate the IRB for SIDCER recognition

By adlai
(161 views)

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