Clinical and behavioral studies are cornerstones of any Premarket Tobacco Product Application (PMTA) submission, from pharmacokinetic to actual use investigations. This webinar will explore the ...
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Operationalizing ADC Clinical Trials: Best Practices for Success, Upcoming Webinar Hosted by Xtalks
Join experts from Premier Research, Ashley Herrick, PhD, Vice President, Oncology Program Strategy; and Jordan Curry, Senior Project Director, Oncology, for the live webinar on Thursday, January 29, ...
In a time when COAs are more nuanced, critical and complex than ever, researchers can turn to best practices to move forward ...
Conducting a definitive QT evaluation is a critical regulatory requirement for small molecule drug development. With evolving ICH guidance and increased interest in early phase QT strategies, ...
Traditional trial start-up workflows often follow a sequential path, from feasibility to contracting, then regulatory ...
Integrated clinical research site organization will use SiteGrades and compliant AI to optimize operations, Resource Allocation, and quality across 30+ sites SiteGrades will unify data from AMR ...
The clinical trials arena is becoming increasingly data-driven, with demand growing for sponsors to have real-time data access and ongoing updates throughout a study rather than just a final report.
CARE-ACE supports autonomy through bounded agentic reasoning, in which diagnostic, prognostic, planning, and risk-assessment ...
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