Products

Pharmaceutical-grade
science at startup
pricing.

90% less than traditional formulation consulting.
20x faster delivery. Full ownership of your formulation.

Formulation Audit

Know exactly where your current formula stands.

$500per SKU
vs. $5,000+ traditional
  • Ingredient form analysis
  • Dosage evaluation
  • Interaction screening
  • Bioavailability assessment
  • Improvement recommendations
  • Executive summary report
Get an Audit
Recommended

Standard License Pack

Complete, manufacture-ready formulation for US and UK markets. You own it.

$7,500one-time
vs. $50,000 to $100,000 traditional
  • Full formulation design
  • Evidence dossier (all 10 deliverables)
  • FDA + MHRA compliance alignment
  • CMO-ready specifications
  • Ceuvita Trust Mark rights
  • QR code science portal
  • 12-month literature monitoring
  • Claims substantiation package
Get Started

Global License Pack

Multi-market formulation: US, EU (EFSA-aligned), and GCC-ready.

$15,000one-time
vs. $150,000+ traditional
  • Everything in Standard, plus:
  • EFSA Article 13.1 claims alignment
  • SFDA/GSO registration documentation
  • Halal-compatible ingredient guidance
  • Multi-language label guidance
  • Priority support
  • Quarterly formulation reviews
  • Market expansion documentation
Get Started
Add-ons

Customize your package

Rush Delivery (5 days)+$2,500
Additional SKU+$5,000
EFSA Claims Support (Article 13.5)From $8,000
GCC Registration PackageFrom $5,000
Halal Certification Guidance+$2,000
Clinical Study DesignFrom $15,000

Ownership Guarantee

Every License Pack grants you full ownership of the formulation. Use it with any manufacturer, in any market. No royalties, no ongoing fees. The science is yours.

Our Commitment

Every supplement on every shelf should be backed by real science.

Ceuvita exists to make pharmaceutical-grade formulation science accessible to every brand willing to hold itself to a higher standard.

Early Access

Join the waitlist.

Join the waitlist for early access to Ceuvita. Pharmaceutical-grade formulation science and regulatory-ready documentation, delivered in 5 to 15 days.

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