Trellis™
Scientific Support for Startup Compliance
We handle your FDA, EPA, and USDA paperwork. You focus on building your business.
Generally Recognized as Safe determination for novel food ingredients and additives.
75-day premarket notification for new dietary ingredients entering the US market.
Pre-manufacture notice for new chemical substances under the Toxic Substances Control Act.
Import, movement, and environmental release permits for regulated biological materials.
Complete a short intake form and upload your lab reports, CoAs, and safety studies.
A vetted PhD scientist, matched to your specific regulatory pathway, is on your project.
Your scientist prepares the full submission, then records a video walkthrough of every conclusion.
Review your filing, ask questions, and submit to the agency with a scientist behind every page.
Not sure where to start? We review your product and tell you exactly which agencies you need to file with and what it will take.
A PhD scientist handles your full FDA GRAS filing from start to finish — structured, reviewed, and submission-ready.
Everything in the full filing, plus an independent panel of three PhD scientists who each review and co-sign your GRAS notice.
Every expert is credential-verified against their published research before being assigned to your project.
Your scientist records a video walking through their conclusions before the filing reaches you.
100% formatting compliance for your pathway. Two free revision rounds if the agency sends an RFI.
The Tier 0 Portfolio Diagnostic fits standard micro-purchase / P-Card limits. Each founder gets a regulatory roadmap; you get an executive summary for your board.
Start with a quick review to find out what you need, or go straight to your full filing.