'Consent document' presentation slideshows

Consent document - PowerPoint PPT Presentation

Objectives

Objectives

Objectives. Identify consent process requirements Distinguish between IRB, PI/Designee consent process responsibilities Identify what went wrong? Summarize tips to avoid deficiencies.

★ ★ ★ ★ ★

579 views • 50 slides
Dr. Anjum Susan John, MRC

Dr. Anjum Susan John, MRC

Dr. Anjum Susan John, MRC. Objectives. What is informed consent ? The ethical justification of informed consent The informed consent process The contents of the consent form The documentation and filing of consent forms. Ethical requirements for any research. Informed consent.

★ ★ ★ ★ ★

730 views • 47 slides
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

★ ★ ★ ★ ★

484 views • 41 slides
Part 1 of 3 Part Series: Informed Consent: The Document

Part 1 of 3 Part Series: Informed Consent: The Document

Part 1 of 3 Part Series: Informed Consent: The Document. Wendy Lloyd, BA, LPN, CIP, CCRP Regulatory Affairs and Compliance Specialist Process Improvement Team. Agenda. Identify consent document requirements Distinguish between IRB, PI and Coordinators consent document responsibilities

★ ★ ★ ★ ★

481 views • 40 slides
Part 1 of 3 Part Series: Informed Consent: The Document

Part 1 of 3 Part Series: Informed Consent: The Document

Part 1 of 3 Part Series: Informed Consent: The Document. Wendy Lloyd, BA, LPN, CIP, CCRP Regulatory Affairs and Compliance Specialist Process Improvement Team. Agenda. Identify consent document requirements Distinguish between IRB, PI and Coordinators consent document responsibilities

★ ★ ★ ★ ★

404 views • 40 slides
Understanding the Process of Documenting Informed Consent

Understanding the Process of Documenting Informed Consent

Understanding the Process of Documenting Informed Consent. Anne Roussell, RN Office of Clinical Research. QA Study Audits. The purpose: provide principal investigators (PI) and study teams early detection regarding study conduct issues;

★ ★ ★ ★ ★

317 views • 31 slides
INFORMED CONSENT

INFORMED CONSENT

INFORMED CONSENT. The Ethical Principle The Regulations The Document The Process What Should It All Mean To Me?. The Ethical Principle. The Belmont Report outlines three basic ethical principles: Respect for Persons Beneficience Justice Which principle supports informed consent?.

★ ★ ★ ★ ★

746 views • 29 slides
INFORMED CONSENT

INFORMED CONSENT

INFORMED CONSENT. The Ethical Principle The Regulations The Document The Process What Should It All Mean To Me?. The Ethical Principle. The Belmont Report outlines three basic ethical principles: Respect for Persons Beneficience Justice Which principle supports informed consent?.

★ ★ ★ ★ ★

378 views • 29 slides
Informed Consent

Informed Consent

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

★ ★ ★ ★ ★

688 views • 27 slides
iRIS

iRIS

iRIS. Top 25 Frequently Asked Questions. Question 25. How do I get my new application signed by a USF Scientific Reviewer and Department Chair?

★ ★ ★ ★ ★

450 views • 27 slides
Procedure Of Taking Informed Consent

Procedure Of Taking Informed Consent

Procedure Of Taking Informed Consent. How will we take consent Written Oral Video. The Consent Process : The subject/representative must enter the date of signature on the consent document, to verify that consent was obtained before the subject began participation in the study.

★ ★ ★ ★ ★

466 views • 23 slides
How to Avoid Problems in the Informed Consent Process

How to Avoid Problems in the Informed Consent Process

How to Avoid Problems in the Informed Consent Process. Shannon Ontiveros, MS, CIP, CIM Institutional Review Board. Agenda. Required elements of consent Additional Elements Writing the Consent Document Reminders to Check Amendments Suggestions for Assent Documents #1 POINT. Research

★ ★ ★ ★ ★

366 views • 22 slides
The New Common Rule

The New Common Rule

The New Common Rule. Overview of Changes to Human Subjects Research Regulations. Seth Hall, JD*, CIP. Interim Director, Human Research Office * I am not an attorney for UMMC. The Common Rule. 45 CFR 46.101, et seq. The Revised Common Rule was published on January 19, 2017

★ ★ ★ ★ ★

216 views • 20 slides
May I have your permission please?

May I have your permission please?

May I have your permission please?. The consent process: What, Where, When, Who and Why. Valerie Smith OHRP IRB Program Manager 327-2370/valeries@unr.edu. The Farside , by Gary Larson . Why?.

★ ★ ★ ★ ★

292 views • 19 slides
Understanding the IRB Process

Understanding the IRB Process

Understanding the IRB Process. Dr. Cheryl Peters, Evaluation Specialist cpeters@anr.msu.edu. Is it research?. Does our Extension project require IRB review? 3 Questions. Is it research?.

★ ★ ★ ★ ★

255 views • 19 slides
Informed Consent: Process, Documentation, Alteration and Waivers

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

★ ★ ★ ★ ★

794 views • 18 slides
Overview of Accreditation Changes

Overview of Accreditation Changes

Overview of Accreditation Changes. Sara Brand Associate Director Research Compliance Administration. Objectives. Communicate recent changes in policies and procedures from recent AAHRPP re-accreditation Detailed Self-Assessment Accreditation Site Visit in December 2007

★ ★ ★ ★ ★

285 views • 14 slides
When Must Clinical Risks be Described in a Research Consent Document?

When Must Clinical Risks be Described in a Research Consent Document?

When Must Clinical Risks be Described in a Research Consent Document?. Ron Kadden - September 10, 2008. The Question. If a research study involves standard-of-care clinical interventions, that are being done for clinical reasons:

★ ★ ★ ★ ★

181 views • 11 slides
Informed Consent Waivers

Informed Consent Waivers

Informed Consent Waivers. IRB Health Sciences & Behavioral Sciences University of Michigan 2009-2010. Goals of this audiocast. Provide an overview of the informed consent waivers permitted by the federal regulations governing research with human subjects (45 CFR 46.116, 46.117).

★ ★ ★ ★ ★

388 views • 10 slides
Chicken Soup for the Busy Coordinator

Chicken Soup for the Busy Coordinator

Chicken Soup for the Busy Coordinator. March 2009. Tip of the Month. Question: Who should I list in the consent document as the contact person for subjects to pose questions to? . Answer.

★ ★ ★ ★ ★

317 views • 5 slides

View Consent document PowerPoint (PPT) presentations online in SlideServe. SlideServe has a very huge collection of Consent document PowerPoint presentations. You can view or download Consent document presentations for your school assignment or business presentation. Browse for the presentations on every topic that you want.