MGH Division of Clinical Research

QI Roundtable: Consent Process

Ended: Dec. 15, 2016

Speaker: Daniel Jones, QI Specialist

Informed consent: it’s more than just a document. Do you know the ethical considerations that factor into obtaining truly informed consent? If your study involves vulnerable populations, such as children, are you knowledgeable of the special protections afforded to them, and the Partner’s policies governing their consent? In this session, Daniel Jones, QI Specialist of the Partners Quality Improvement Program will discuss these issues and how to fulfill the Partner’s policies for documenting the informed consent process. He will describe the informed consent process, review vulnerable populations, the special protections afforded to them, and how these apply to the informed consent process, and discuss how to effectively comply with the Partners policies for documenting informed consent.

This session is limited to 25 participants to facilitate interaction.
Registration is required. Please contact Tiereny Morrison-Rohlfs at tmorrison-rohlfs@partners.org with any questions.

Programs:
Clinical Research Investigator Beginner Clinical Research Coordinator

Categories:
Clinical Research Research Quality Improvement

Sponsor:
MGH Division of Clinical Research

Sessions

Dec. 15, 2016 12/15/16
12PM-1PM 		12 PM – 1 PM
Garrod/Mendel, Floor 2, Simches Research Center

Other Offerings

Past Offerings
QI Roundtable: Consent Process Jan. 23, 2018 01/23/18

Reviews

Ariela M: professional, on point, clear and very knowledgeable instructor
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Date Attended: Jan. 23, 2018, 10:57 a.m.
Date Reviewed: Jan. 24, 2018, 10:02 a.m.
Anonymous:
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Date Reviewed: Jan. 23, 2018, 12:18 p.m.
Anonymous: This course should have been longer than an hour in order to cover all of the material! Instructor was very kind and knowledgeable, and the powerpoint was very informative. Not much time left for discussion and questions, though.
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Date Reviewed: Jan. 23, 2018, 12:14 p.m.