FDA and EMA require uncertainty quantification. Credible intervals are native to Bayesian output. Small-sample efficiency, interpretability, and the ability to formally incorporate clinical prior beliefs make Bayesian methods the natural fit for pharma and biotech.

We basically have clients in two industries: marketing, and biotech.

Work in This Space

Roche

Successfully fit a 34K-parameter model on 250K observations in just over 1 hour using JAX/NumPyro GPU-accelerated inference.

GenomicsGPUHierarchical Bayesian

Takeda

Bayesian digital twin for a 28-day CAR-NK cell manufacturing pipeline. Stage-by-stage state space model enabling real-time prediction from day-6 measurements.

Digital TwinCell TherapyManufacturing

Akili Interactive

Bayesian psychometric modeling for EndeavorRx — the first FDA-approved prescription video game for ADHD treatment.

Digital TherapeuticsClinical TrialFDA

Trusted By

  • Roche
  • Takeda
  • Akili Interactive
  • Erisyon
  • Haleon
  • Syngenta
  • IQVIA
  • Procter & Gamble

What We Solve

Clinical Trial Analysis

Hierarchical Bayesian designs for dose-response, PK/PD modeling, patient outcomes with longitudinal data, and biomarker estimation with regulatory-defensible uncertainty.

Drug Manufacturing Digital Twins

Cell therapy manufacturing process modeling with real-time prediction from early-stage measurements. Stage-by-stage Bayesian state space models for CQA tracking.

Genomics & Large-Scale Bio Data

Large-scale hierarchical Bayesian models validated at 34K parameters and 250K observations. GPU-accelerated inference via JAX/NumPyro in approximately 1 hour.

Digital Therapeutics

Ordinal regression for clinical assessment instruments. Bayesian psychometric modeling for cognitive constructs and latent variable modeling for digital biomarkers.

Why Bayesian

Why Bayesian for Pharma & BioTech?

  • Regulatory defensibility — FDA/EMA require uncertainty quantification. Credible intervals are native to Bayesian output. Models pass regulatory validation where black-box ML fails.
  • Small sample efficiency — Hierarchical models work with as few as 17 donors. Partial pooling borrows strength across sparse cohorts without discarding data.
  • Interpretability — Biotech and pharma need to explain predictions to regulators and clinicians, not just make them. Every parameter has a clear scientific meaning.

“We wanted to draw big conclusions from a big set of data. This is by far the most successful collaboration I’ve seen — and I’ve had many consultants.”

Titi Alailima
VP of Applied Data, Akili Interactive

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