If a specific asset is on your desk, we spend the time on it: who adopts it in real practice, the target population you can defend, and how it clears the European reimbursement gate.
SPinsights maps who will adopt a therapy in real multidisciplinary practice, qualifies and prioritises the experts who decide access, defines the target population you can defend in front of them, and reads the European market access and early access path before submission. Not advising on medical affairs and market access. Building them, including the real-world evidence and health economics that payers expect.
You raised on the strength of the mechanism, and the science holds. The next round will not ask about your biology. It asks who adopts this in a multidisciplinary practice, what the target population is, how it fits the patient journey, and whether a well-defined unmet need would push Europe to grant early access before approval. The first time a patient received an advanced therapy taken through early access, the real job was clear: turning a mechanism into a prescription, in a real clinic, in a specific country.
Early-stage oncology and rare-disease biotechs, usually scientific founders who need senior judgment before hiring a chief medical officer. Also pharma clinical development, market access and medical affairs teams preparing future launches.
If you want a large agency with a junior team, or a logo on a slide. Clients value discretion and compliance. Your name stays yours, by design.
Twenty to thirty minutes, on your asset, with the person who would do the work.
Start with the framework: the nine-section read on who adopts and how an asset clears the European reimbursement gate.