Ended: July 19, 2018
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? Are you aware of federal regulations and IRB policies regarding informed consent? In this session, we will discuss these issues and how to comply with federal regulations and IRB policies for documenting the informed consent process.
Participants are welcome to bring lunch. Registration is required. If you have any questions, please contact dcredu@partners.org
Programs: QI Bootcamp Beginner Clinical Research Coordinator
Category: Research Quality Improvement
Sponsor: MGH Division of Clinical Research
The application period is closed. Please check back for future offerings.
Sessions
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July 19, 2018
07/19/18 12PM-1PM |
12 PM – 1 PM |
Garrod/Mendel, Floor 2, Simches Research Center
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