AI-Powered Regulatory Compliance Intelligence

Email briefs and a SaaS dashboard that keep mid-market companies ahead of regulatory changes — without the six-figure compliance budget.

The Compliance Problem

Mid-market companies face the same regulatory burden as enterprise — without the resources to match.

US companies must monitor regulations

Average fine per missed deadline

Annual cost of lobbyists

Annual cost of a compliance analyst

Two products, one mission: keep you compliant.

Regulatory changes distilled into clear, actionable email briefs within 2-4 hours of publication.

Every brief is reviewed by compliance professionals before reaching your inbox. No hallucinations.

Each brief includes specific steps your team needs to take, with deadlines and responsible parties.

Track compliance tasks across your team with our SaaS dashboard. Never miss a deadline.

Assign tasks, share briefs, and collaborate with your compliance team in one place.

Stay on top of regulatory changes from anywhere. Briefs are optimized for mobile reading.

Purpose-built for regulated mid-market companies.

FDA regulations, drug safety reporting, clinical trial compliance

510(k) submissions, post-market surveillance, UDI requirements

SEC filings, AML/KYC requirements, state licensing deadlines

HIPAA updates, CMS rule changes, state health regulations

FDA labeling rules, FSMA compliance, import regulations

Get AI-powered regulatory intelligence delivered to your inbox — reviewed by humans, built for your industry.