How it works
From a five-minute form to full US-market compliance — here is exactly what happens.
- 1
Tell us about your products
You complete a short form about your products, facilities, and target timeline. No documents are required to start.
- 2
AI gap analysis, expert-reviewed
Our platform runs a gap analysis against MoCRA and FDA requirements for your exact situation. A regulatory specialist reviews the results and walks you through them in a free consultation.
- 3
We file, represent, and monitor
Once you engage us, we prepare and submit filings, act as your US Agent where needed, and monitor deadlines and status year-round.
AI speed. Human accountability.
Our platform accelerates the work. Our specialists own the result.
What our AI does
- Pre-checks labels and ingredient lists against FDA rules in minutes
- Monitors registration status and deadlines around the clock
- Drafts filings in minutes, not weeks
What our experts do
- Review and sign off on every filing
- Handle all FDA communications
- Own the edge cases that need human judgment
Enter the US market with confidence.
Get a free compliance assessment from our specialists — no obligation.
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