Let Regulaido handle the groundwork. Make room for what matters.
Regulaido is an agentic AI platform for Medical Writing, with specialized agents for research, systematic reviews, document editing and review.
Already at work.
Used daily by medical writers, HTA analysts, and regulatory teams across Europe.
Measurable capacity gains across the writing team.
“Regulaido gives me the opportunity to focus on strategic assessments and at the same time extracts fast as well as accurate clinical trial information.”
What you can hand over.
Delegate time-intensive regulatory and market-access tasks directly in your existing files and templates.
More time for your expertise: scientific judgement, strategy, and final sign-off.
Your work stays connected. From source to final document.
Research, evidence, writing and review are often handled in separate steps, making it harder to trace information back to its source. Regulaido connects the entire workflow, keeping sources, evidence and claims traceable as work moves from one stage to the next.
Research
Find and analyze relevant sources.
Evidence
Structure findings and keep them linked.
Writing
Use existing evidence directly in your documents.
Review
Check and refine with full context.
We are Pharos Labs.
Pharos Labs is the team behind Regulaido. We've been developing Regulaido together with Medical Writers from the start. Their experience and feedback continue to shape the product today.
Europe 2026Presenter · Vienna
We stay close to the people who use Regulaido every day.
Events & latest research
All research & events →
Meet us at ISPOR Europe 2026 in Vienna (Poster HTA86)
Presenting HTA-Bench: Regulaido achieves the #1 Pareto-optimal score (72.8 vs. 67.3 Codex CLI and 51.5 Claude Code) in 26 minutes.
AI in JCA dossiers: the EU's new HTACG rules explained
The HTA Coordination Group now expects prompts, model versions, and human verification steps to be logged for Joint Clinical Assessments.
From Word SmPC to EMA FHIR ePI XML in 3.5 minutes
Converting an approved EMA Summary of Product Characteristics into a validated FHIR XML bundle in one workflow.
What would you hand over first?
Research? A systematic review?
A document that needs another round of review?
See how Regulaido works with the tasks already on your desk.