Specialists with deep domain roots.
Trelice is a specialist software company for clinical trial documentation. We build for the medical writers, clin-ops leads, and biostatisticians who can’t afford a sprawling all-in-one platform where protocol authoring is just one slice.
Every trial document written once. Propagated, defensible, and patient-readable by default.
Clinical protocols are the blueprint for every downstream document a trial produces. For decades they’ve been written in Word, cross-referenced by hand, and re-synced by heroic effort whenever anything changes.
We think software should carry that load. A structured protocol with the regulatory rationale baked into every field, every change propagating across linked sections, and the output rendering live in a submission-ready Word template. That’s the baseline we’re building toward.
How we work.
Specialist, not suite
We do protocol authoring and consent generation. We don’t do EDC, CTMS, or eTMF. Depth over breadth.
Regulatory by construction
Every field knows the ICH/FDA/EMA guidance it answers to. Compliance is a property of the schema, not a late review step.
Editorial, not enterprise
Serious software for serious work. No dashboards for dashboards’ sake. Whitespace, type, and the thing that mattered.
Specialists with deep domain roots.
Ilan Slonim
15+ years in software leadership across startups and enterprises in multiple regulated industries.
Danielle Wall
Harvard B.S. Neurobiology. 15+ years of clinical research and innovation for industry leaders globally (Gilead, Tanabe).