Ended: Aug. 2, 2018
Per Federal Regulations, Good Clinical Practice, and IRB policies, investigators and research staff are required to keep case histories on enrolled subjects. In this session, we will review requirements for source documentation and record keeping of subject files. The presentation will include a hypothetical protocol with enrolled subjects and its appropriate source documentation.
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
Aug. 2, 2018
08/2/18 12PM-1PM |
12 PM – 1 PM |
Garrod/Mendel, Floor 2, Simches Research Center
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