Archives: Resources
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.
The 2025 FSP Trends Report
Maximize FSP engagements to meet your timelines and explore the latest trends report.
FSP Site Support solutions
Overcome site challenges and meet timelines.
Transitioning pharmacovigilance services to a single FSP partner
This white paper shows the value of consolidating PV services to a single FSP partner and how they can overcome related challenges.
Registries: Supercharging Real-World Evidence for Drug Development and Approval
Learn how RWE and RWD from registries enhance drug development and approval for rare diseases.
AI and Digitization in Clinical Research and Medical Writing Series
Explore AI and digitization in clinical research and medical writing, learning from experts on efficiency, real-world success, and prospects in this video series.