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Fixed price. No retainer. A scientist on your project within 48 hours.
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 and upload your lab reports, Certificates of Analysis, and safety studies.
A vetted PhD scientist, matched to your specific regulatory pathway, is on your project. Typical delivery: 3–6 weeks from complete intake.
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.
Find the right agency, audit your lab files, and get a clear roadmap before you spend runway on the wrong path.
Already have a scientific draft? Get independent PhD validation and sign-off without buying a full dossier sprint.
A PhD scientist structures your full filing — APHIS, TSCA, NDI, GRAS, or multi-geography novel food — submission-ready.
Full product list, add-ons, and FAQs → FAQ catalog. Need a W-9 or formal invoice? Buyer center.
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.
Formatting and required-section compliance for your pathway. Two free revision rounds for structural RFIs — not a promise of agency approval.
Put technical assistance funds to work for your emerging ag and biotech companies. For $5,000 per company, each team gets a clear report on which agencies apply, what data is missing, and what to do next — in three weeks.
Start with a quick review to find out what you need, or go straight to your full filing.