---
title: "About | Trelice"
description: "Trelice is an ICH M11-native platform for sponsors, CROs, and research sites to author clinical trial protocols and generate aligned downstream documents."
canonical_url: "https://www.trelice.com/about"
---

About

# 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.

Mission

## 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.

Values

## How we work.

01

### Specialist, not suite

We do protocol authoring and consent generation. We don’t do EDC, CTMS, or eTMF. Depth over breadth.

02

### 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.

03

### Editorial, not enterprise

Serious software for serious work. No dashboards for dashboards’ sake. Whitespace, type, and the thing that mattered.

Team

## Specialists with *deep domain roots.*

![Ilan Slonim](/images/team/ilan-slonim.png)

### Ilan Slonim

CEO & Founder

15+ years in software leadership across startups and enterprises in multiple regulated industries.

![Danielle Wall](/images/team/danielle-wall.png)

### Danielle Wall

Advisor

Harvard B.S. Neurobiology. 15+ years of clinical research and innovation for industry leaders globally (Gilead, Tanabe).