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.
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Learn more about SC CTSI's Team Science Workshop that took place on September 26th, 2019
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The pilot study is the first to be completed under a novel academic-government collaboration between the SC CTSI, the UCLA CTSI, and the Los Angeles County Department of Health Services
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An educational video for emerging researchers provides info on designing research studies, applying for grant funding, and navigating institutional processes.
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A large study conducted by USC assistant professor Judy Pa shows that living a healthy lifestyle can reduce the risk of Alzheimer's or other dementia, even if you have a genetic risk.
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For decades, clinical research studies underrepresented non-white populations, leaving important knowledge gaps. But medical dermatologist Iris Z. Ahronowitz, MD, and her team used a wealth of data at USC for a first-ever retrospective study involving a majority Hispanic population of solid organ transplant recipients.
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Spring 2018 Pilot Awardee, Min Yu, MD, PHD on the potential of using circulating tumor cells to monitor brain metastasis
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Sharing expertise across universities adds value to pilot funding programs
Read moreNIH Funding Acknowledgment: Important - All publications resulting from the utilization of SC CTSI resources are required to credit the SC CTSI grant by including the NIH funding acknowledgment and must comply with the NIH Public Access Policy.