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Webinar | From Feasibility to Data Confidence: Enhancing Evidence Synthesis Through Global Best Practice and Visualization
Join us for a focused, practical session that breaks down how to conduct high-quality feasibility assessments (FAs) that support robust evidence synthesis, that meets diverse HTA markets. Drawing from guidance across leading HTA bodies including CADTH, EU HTA CG and IQWiG, introducing step-by-step tools and visualization techniques to help you plan with greater clarity, reduce uncertainty, and align internal teams more effectively.
Register here
Webinar | Database Studies & Medical Chart Reviews
As demand for real-world evidence (RWE) grows among regulators and HTAs, study sponsors face key decisions around data sources and study design. This webinar will address how to choose fit-for-purpose data, weigh the pros and cons of different RWE types, leverage data linkages and synthetic data, and streamline global research efforts.
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Webinar | European JCA: Early PICO Simulation & Planning of national HTAs
The European JCA is already a reality for oncology and ATMP submissions—and other drugs will follow soon. It won’t replace national HTAs, but adds another layer of requirements.
Learn what’s needed for early JCA planning, from PICO scoping to comparative evidence options.
ISPOR Europe 2025 - Glasgow, Scotland | November 9-12
See you at ISPOR Europe 2025!
Join us at ISPOR Europe 2025 in Glasgow! We will be showcasing our unique tools, designed to bring innovative solutions to market access and real-world evidence challenges.
Let’s connect!
Webinar | Maximizing the Value of your RWE Program: Strategic Planning for Global Database Studies
With constrained resources, it’s essential to align your global database strategy with your evidence planning needs. However, the landscape of RWE data available across key markets is large, diverse, and ever-changing. How can your team best generate evidence needed in the US and Europe in this challenging environment?
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Webinar | US Regulatory Approval & Successful Payor Negotiations
The US FDA and payers are increasingly using real-world evidence (RWE) to support regulatory approvals, formulary positioning, and label expansions. This webinar explores how sponsors can efficiently apply RWE across the product lifecycle, align with FDA guidance, integrate it into clinical trials, and navigate payer and regulatory expectations—plus insights on the Inflation Reduction Act.
Register here
Webinar | Global Evidence Generation Planning: Approaches and options
Early Evidence Generation Planning goes beyond clinical trials—it includes RWE, external controls, endpoint validation, and more. This webinar explores how to assess needs early and build a tool-driven, integrated evidence plan for regulatory and HTA success.
Register here
ISPOR 2025 - Montreal, QC, Canada | May 13-16
See you at ISPOR 2025
Join us at ISPOR 2025 in Montreal, QC, Canada! As specialists in market access and real-world evidence, we’ll be showcasing our unique tools designed to provide innovative solutions that support your healthcare journey.
Let’s meet!