Archives: Resources
Biosimilar development brochure
Accelerate clinical trials with our expertise in biosimilar development.
How digitized protocols accelerate clinical research
Discover how digitized protocols are transforming clinical research. Learn about the benefits of digital clinical trials, including improved efficiency, data accuracy, and faster timelines.
The 2025 State of FSP Outsourcing: Challenges, Trends and Opportunities, and the Future of FSP Strategies and Models
Discover how FSP and hybrid FSP/FSO models are helping sponsors better navigate clinical development outsourcing.
Real-world evidence studies – Diverse Data Designs
In close collaboration with sponsors, we identify and understand multi-stakeholder evidence needs across the product lifecycle.
US inflation reduction act: pipeline considerations
A risk exposure framework for drug developers.
Navigate the EU HTA Regulation
Trusted partner with 30+ years of experience in EU HTA, aiding health tech developers through EU HTA Regulation complexities.
Registries and Real-world Evidence
Customizable registry solutions for actionable insights, tailored study design, and regulatory-grade data to accelerate development.
Peri- and Post-approval Safety and Real-world Insights
Learn how we optimize post-authorization safety obligations with a holistic, collaborative, and custom study design approach.
