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Legal Aspects of Clinical Trials Discussed at Recent Regulatory Science Boot Camp/Symposium
Principal investigators and regulatory professionals must stay up-to-date with numerous legal requirements and strategies pertaining to clinical studies. These include U.S. Food and Drug Administration (FDA) forms, contracts with sponsors, liabilities, indemnifications, special use protocols, and inventions to protect. And then there are international laws.
Read moreUndergraduates Take Career Strides in SC CTSI's Regulatory Knowledge and Support Core—and Beyond
Research by undergraduate students has led to presentation opportunities and new career paths.
Read moreSC CTSI Symposium Illuminates Complex World of Regulatory Science for Clinical Researchers
A day-long boot camp helps investigators understand the key steps and issues – as well as the potential benefits – in the fast-changing regulatory environment of clinical trial start-ups.
Read moreSC CTSI Co-Director Urges Young Women To Study STEM Subjects
Michele Kipke, PhD, SC CTSI co-director, speaks at "Women in STEM: Designing, Discovering and Delivering Change.
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