Ended: Aug. 16, 2018
Many drug and device clinical trials are conducted at Partners Institutions. Study teams have the option of using the investigational drug service to manage study drug accountably or storing and managing accountably onsite. For device trials often the only option is onsite storage. Study teams must be aware of the regulatory requirements for drug and device accountability as well as Partners policies for storing drugs/devices on site. In this session, we will discuss the regulations applicable to drug and device accountability, Partners polices for onsite storage and how to avoid noncompliance.
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
| Investigational Product Accountability: What is this and How do I do it? |
Aug. 16, 2018
08/16/18 12PM-1PM |
12 PM – 1 PM |
Garrod/Mendel, Floor 2, Simches Research Center
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