Ended: March 28, 2019
Every study should have a regulatory binder or file whether survey research or drug/device clinical trials. There is a standard set of documents referred to as “essential documents” that should be filed and maintained in the regulatory binder. In this session, we will discuss regulations applicable to documentation, which documents are considered essential, how these documents should be stored, for how long and where.
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
Sessions
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March 28, 2019
03/28/19 12PM-1:30PM |
12 PM – 1:30 PM |
Garrod/Mendel, Floor 2, Simches Research Center
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Other Offerings
| Past Offerings | |
|---|---|
| Maintaining a Regulatory Binder is not as Easy as it Seems! |
Aug. 23, 2018
08/23/18 |