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Therapeutic Areas

Whatever your area, we have built it before.

Oncology, cardiology, rare disease, immunology, neurology, and more. The science changes from one area to the next; our job is to have seen enough of yours to get it right the first time. We do the heavy lifting.

Across the areas of teams at Roche Amgen Novartis Bristol Myers Squibb Regeneron Takeda
Find your area

Your therapeutic area is not new to us.

Pick an area and see the kind of indications we have already built the science for. You bring the area and the evidence. We do the heavy lifting.

Oncology

The endpoint story a tumor board actually debates, built from your own readout.

Where teams here usually start →
Why breadth matters

The heavy lifting is knowing the science already.

The slowest part of a project is the ramp: learning the mechanism, the endpoints, the way your specialists think. When we have worked the area before, that ramp is already behind us.

You bring the publication and the therapeutic-area context. We bring the pattern of having built it before, and we do the mapping and the build.

We speak the specialtyThe right terms, the right emphasis, the way the physician expects to hear it.
Accurate the first timeFewer review rounds, because the science was right before it reached your desk.
Ready for the next indicationOnce we know your area, the second and third projects move faster.
Same platform, different first stop

One publication. A cardiologist and an oncologist. Two first stops.

Two specialists open the same approved publication in the same experience. Tap one and watch where their journey starts. Neither reads the other’s field first, and it is all one MLR review.

Your area’s publication, openedOne source. One review. One link.
The cardiologistHer first stops in the experience
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Same publication, two specialties, one review. Each first stop recombines modules that were already approved, so no new claim is created and one MLR pass covers every area’s route. That is how one experience stays personal in every field.
The Impact Gap Report · 2026 FREE

Pharma keeps publishing. Physicians stopped reading.

60+ studies, side by side: why your best science never reaches the physicians it was written for, and what the evidence says actually works instead.

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57 pages · every number sourced · straight to your inbox
Any area, the same three products

Whatever the area, the products do not change.

The therapeutic area changes the science. It never changes how the science lands. You bring the area and the evidence. We do the heavy lifting.

Every area, the same standard.

Breadth never means a lower bar. Whatever the area, every frame maps to your approved source, so the work is built for MLR from the first frame, in every field we touch.

0new claims, in every area we touch. Your evidence, only clearer.
30+languages from one approved core.
1MLR review covers every version, not per asset.
“They knew our endpoints before we finished explaining them.”
Medical Affairs Lead · Rare Disease
See it in your field

Tell us your area.

Name the area and send the science. We will show you what we have built in fields like yours and what your evidence would become. On the house. No promises.

Questions

Frequently asked questions

Rare and specialist areas are where the heavy lifting matters most. We start from your approved science, and the harder the field, the more the accuracy and the speed of not starting cold are worth.

We work across therapeutic areas, so the terms, the endpoints, and the way your specialists think are usually familiar. Where they are not, we learn them from your source before anything is built.

Yes, and it gets faster as we go. Once we know your area, the second and third indications build on what we already understand, without starting the science over.

We will not tie it to a fixed date. You approve the core the normal way, at script, storyboard, and final animation. From there, that same approved core carries every version, so new cuts and languages do not restart the scientific review. The overall pace tracks your own review, which we plan around with you from day one.

Always. In every area, every frame traces to an approved claim, so the work is structured for MLR from the first frame and fits your existing Veeva workflow.