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What is the role of Data and Safety Monitoring in Clinical Research Involving Human Subjects - When and How? - Webinar By MentorHealth
Webinar in-person 28th to 28th May 2013 Fremont, California, United States of America Website: http://alturl.com/awgyv Contact person: Roger Steven Overview: All Clinical Research protocols have a prominent safety monitoring plan as part of the overall research plan / protocol. This "plan" is to ensure the safety of participating subjects and to ensure the validity and integrity of the data. Deadline for abstracts/proposals: 28th May 2013 Check the event website for more details. View all events from this organizer.
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