Predicting drug bioequivalence from messy clinical PDFs, starting from a HIPAA foundation.
GenRx had a bold idea: predict drug bioequivalence from messy clinical PDFs. But an idea isn't an architecture, and investors fund what they can see.
They needed to walk into a funding round with a secure, working AI architecture, not a slide.
We started with the foundation, a HIPAA-aligned environment on AWS, before a single prediction ran.
An engine that reads unstructured clinical PDFs (NLP), predicts the key pharmacokinetic metrics (PyTorch), investor-ready.
5.0 / 5.0 on Clutch, quality, schedule, cost.
In regulated domains, the model is the easy part. The architecture that makes it safe and credible is the product.
A high-volume assembly line that still picked parts by hand off paper lists.
A macOS compliance agent that ran fine interactively, but wasn't something they could ship.
A US gateway provider drowning in bespoke processor integrations.
A US B2B services operation running on disconnected systems with no single source of truth.
A Singapore innovation ecosystem matched startups to investors by hand.
TELEMED2U needed to scale remote care, but consultations were inefficient and costs were climbing.
A clinic network running on siloed records that couldn't keep up as it grew.