Ethics and Clinical Research Protocols
Sponsored by the MGH Division of Clinical Research
Melissa Frumin, M.D., M.S., Chair, Partners IRB
In this course, participants will receive an overview of the ethical foundation of Human Subject Protection in clinical research. This will be done through case studies of typical protocols that have come before the Partners IRB. These cases will raise issues of risk/benefit, surrogate consent, research with children, decisionally impaired subjects and medical record review.
This lecture is strongly recommended for all investigators and study staff.
Registration is required. Please contact dcredu@partners.org with any questions.
Programs: Beginner Clinical Research Coordinator Experienced Clinical Research Coordinator
Categories: DCR Spotlight Ethical Oversight
Sponsor: MGH Division of Clinical Research
Modules
Ethics in Clinical Research |
Past Offerings
Ethics in Clinical Research | July 11, 2017 |
Ethics in Clinical Research | July 25, 2018 |
Reviews
Date Reviewed: July 26, 2018, 8:25 a.m.
Date Reviewed: July 25, 2018, 3:01 p.m.