How It Works

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.

5–15 days
01
Step 01

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.

1 to 2 days
02
Step 02

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.

2 to 5 days
03
Step 03

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.

1 to 2 days
04
Step 04

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.

1 to 3 days
05
Step 05

Manufacturing Handoff

Your CMO-ready specifications include complete ingredient details, quantities, suggested suppliers, and process guidance. Most manufacturers can begin production immediately.

Immediate
06
Step 06

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.

Ongoing
5 to 15 daysFrom concept to manufacture-ready
What You Receive

10 complete deliverables

Every document your manufacturer, regulatory team, and marketing department needs.

Core Deliverables
01

Formulation Spec

Exact ingredients, forms, and quantities your manufacturer needs to produce.

02

Evidence Dossier

Published clinical studies backing every ingredient, dose, and health claim.

03

Safety Analysis

Full screening of ingredient interactions and contraindications, ingredient to ingredient and ingredient to drug.

04

Bioavailability Report

Analysis of how each ingredient absorbs, with form selection optimized for bioavailability.

Complete Package
05

Regulatory Documents

Claims substantiation and regulatory alignment for your target markets (FDA, EFSA, MHRA, SFDA).

06

Manufacturing Brief

Manufacturing specifications your CMO can use to start production immediately.

07

Label Guidance

Supplement Facts panel layout and marketing claims copy, written to pass regulatory review.

08

Competitive Analysis

Competitive landscape analysis showing how your formula stacks up against what's on the shelf.

09

Trust Mark Rights

QR-scannable verification badge consumers can check to see the science behind your product.

10

12-Month Monitoring

We monitor new research for 12 months and alert you if anything changes the science behind your formula.

The Technology
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Top pharmaceutical companies use DeepCeutix, an agentic AI platform, to design drug formulations. Its autonomous research agents cross-reference FDA, PubMed, and ClinicalTrials.gov in real time. Now, that same pharmaceutical-grade science powers every Ceuvita formulation.

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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