'Continuing review' presentation slideshows

Subpart A Subcommittee (SAS)

1.41k views • 130 slides

Subpart A Subcommittee (SAS)

1.18k views • 99 slides

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.

1.08k views • 96 slides

Wayne State University Detroit, MI

864 views • 73 slides

2013 Certification Drive-in Conference

866 views • 72 slides

779 views • 61 slides

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.

660 views • 51 slides

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.

619 views • 46 slides

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.

680 views • 46 slides

Town Hall Q&A Session

528 views • 38 slides

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

554 views • 38 slides

Welcome to IRBManager!

706 views • 36 slides

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.

510 views • 32 slides

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?.

542 views • 31 slides

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

297 views • 29 slides

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.

393 views • 27 slides

Budgeting for Clinical Trials

526 views • 26 slides

Ethical Factors in the Recruitment and Retention of Research Participants

469 views • 23 slides

Continuing Review

374 views • 21 slides

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.

282 views • 15 slides