Archives: Resources
EU Health Technology Assessment Regulation (HTAR)
Learn about the new EU Health Technology Assessment that is intended to make innovative health technologies more widely available and ensure resource efficiency.
Automating Model Building and Statistical Analyses
Actionable insight on using automation for the development of health economic models and statistical analyses.
Bringing clinical trial enrollment to the point of diagnosis
Examine strategies to close the gap between diagnosis and participation
Enhancing vaccine clinical trials participation among elderly
Discover the rising participation of the elderly in clinical trials, their challenges, and successful enrollment methods. Learn more in this insightful paper.
Harnessing Data to Devise Patient-Centric Trials
This on demand video recording will explain how applying the right data strategies can help you design a truly patient-centered trial experience
Radiopharmaceutical Clinical Trials Best Practices
Explore the complexities of radiopharmaceutical trials and the considerations to successfully execute them
Optimizing next-generation sequencing for precision oncology trials
Explore strategies that drive success in precision oncology to improve patient outcomes
How an FSP PV partner helps ensure global compliance
Learn more about how an FSP PV partner help keep up with the evolving regulatory landscape.
Making the Grade: Registries as Sources of Regulatory-Grade RWE
Discover how registries are emerging as valuable sources of regulatory-grade real-world evidence (RWE) to support healthcare decision-making and regulatory submissions.