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 nine-module suite where protocol authoring is 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 — and 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, the golden thread propagating every change, and the output rendering live in a regulatory-compliant 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 isn’t a review step — it’s a property of the schema.
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).