01 Recruiting the Unfindable
When the entire eligible population would fit in one room.
Some conditions are so rare the qualified specialists worldwide number in the dozens — the neurologists and pulmonologists working in areas like ALS and pulmonary arterial hypertension. Panel houses working off purchased lists come back empty, or pad the slate with near-misses. We source each specialist by name and screen them against every clinical criterion. Anyone who does not fit does not count.
Result Every seat filled with a true qualifier, on timeline — no stretches, no substitutes.
02 One Study, Three Continents
One program. Every market on the same clock.
A hospital-based technology needed a global read, fast — across North America, Europe, and the Middle East. Different languages, different regulatory rules, and physicians, nurses, and clinical-operations leaders to reach in every market. Most firms run these as separate studies and stitch them together after the fact. We ran it as one, fielded in parallel, with a single team accountable for the whole recruit.
Result One comparable dataset across every market, fielded at once — a true global read, not a stack of single-country snapshots.
03 Research That Meets the Regulatory Bar
Human-factors work built for scrutiny, not just insight.
Device usability studies get read by regulators, not just researchers. So we recruit the actual users of the device — anesthesiologists, critical-care physicians, surgeons, operating-room nurses, and biomedical engineers — never a convenient stand-in. We run the sessions against recognized human-factors standards and document them to hold up under review.
Result Evidence the client can act on — and defend — when it feeds design and regulatory decisions.
