From concept to
manufacture-ready
in days, not months.
Our computational chemistry platform analyzes thousands of clinical studies to deliver pharmaceutical-grade formulation science in days.
Discovery & Analysis
We analyze your target market, desired claims, competitive landscape, and regulatory requirements. Our computational chemistry platform reviews thousands of clinical studies relevant to your formulation goals.
Formulation Design
Using pharmaceutical-grade methodology, we select optimal ingredient forms for bioavailability, determine evidence-based dosages, and check every interaction. Every decision grounded in published research.
Safety & Compliance Review
Full interaction analysis, contraindication review, and regulatory compliance check. We align with FDA (US), EFSA (EU), MHRA (UK), and SFDA (GCC) requirements based on your target markets.
Documentation Package
You receive 10 complete deliverables: formulation spec, evidence dossier, safety analysis, bioavailability report, regulatory docs, manufacturing brief, label guidance, competitive analysis, Trust Mark rights, and 12-month monitoring.
Manufacturing Handoff
Your CMO-ready specifications include complete ingredient details, quantities, suggested suppliers, and process guidance. Most manufacturers can begin production immediately.
Trust Mark & Launch
Display the Ceuvita Trust Mark on packaging and marketing. Consumers can scan the QR code to access plain-language science explanations. You own the formulation outright.
10 complete deliverables
Every document your manufacturer, regulatory team, and marketing department needs.
Formulation Spec
Exact ingredients, forms, and quantities your manufacturer needs to produce.
Evidence Dossier
Published clinical studies backing every ingredient, dose, and health claim.
Safety Analysis
Full screening of ingredient interactions and contraindications, ingredient to ingredient and ingredient to drug.
Bioavailability Report
Analysis of how each ingredient absorbs, with form selection optimized for bioavailability.
Regulatory Documents
Claims substantiation and regulatory alignment for your target markets (FDA, EFSA, MHRA, SFDA).
Manufacturing Brief
Manufacturing specifications your CMO can use to start production immediately.
Label Guidance
Supplement Facts panel layout and marketing claims copy, written to pass regulatory review.
Competitive Analysis
Competitive landscape analysis showing how your formula stacks up against what's on the shelf.
Trust Mark Rights
QR-scannable verification badge consumers can check to see the science behind your product.
12-Month Monitoring
We monitor new research for 12 months and alert you if anything changes the science behind your formula.
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.