News and Insights

Making the Value Case

Why the Old Drug Development Model Is Breaking Down — And What Comes Next

Rising evidentiary standards, pricing pressure and policy changes are redefining what it takes for pharmaceutical products to succeed. Pharmaceutical companies must rethink how R&D decisions are made, ensuring that clinical trial designs reflect the kind of evidence required for access and optimal reimbursement. Unfortunately, in too many companies, clinical development…

Prioritizing Evidence Generation for Impact

Across the globe, medical device and diagnostic companies are experiencing new levels of price resistance and competitive pressure. No one wants to spend more than they already do – unless they’re given a compelling reason. The only counter to that pressure is compelling evidence of differentiated value. Once considered nice-to-have,…

Optimizing Global Launch Sequencing

Traditionally, launch sequencing has been guided by market size, eligible patient population, and the likelihood of securing market access and adoption. While these criteria are still important, they’re no longer sufficient. Growing budget constraints, more stringent evidence requirements, and the rise of external reference pricing and transparency are forcing pharma…

Prioritizing Real-World Evidence Generation For Impact

Across the globe, pharma companies are experiencing new levels of price resistance and competitive pressure. No one wants to spend more than they already do – unless they’re given a compelling reason. The only counter to that pressure is compelling evidence of differentiated value. Once considered nice-to-have, real-world evidence (RWE)…