What you need to know about pharmaceutical-grade formulation science.
Ceuvita is a formulation science platform that provides supplement, nutraceutical, and botanical brands with pharmaceutical-grade formulation services. We combine computational chemistry, clinical evidence analysis, and regulatory expertise to create science-backed formulations.
Traditional consultants charge $50,000 to $100,000+ and take 6 to 12 months. Ceuvita delivers the same quality (often better, with deeper evidence documentation) in 5 to 15 days at 90% lower cost. Our computational approach analyzes more clinical studies than any human consultant could review manually.
Third-party testing (NSF, USP, ConsumerLab) verifies what's IN your product. Ceuvita documents WHY your formulation is designed the way it is. Both matter, but only one explains the science to consumers and regulators.
A complete License Pack includes 10 deliverables: Formulation Spec, Evidence Dossier, Safety Analysis, Bioavailability Report, Regulatory Documents, Manufacturing Brief, Label Guidance, Competitive Analysis, Trust Mark rights, and 12-month monitoring. From concept to manufactured product.
Standard License Packs are delivered in 5 to 15 business days, depending on formulation complexity. Rush delivery (5 days) is available for time-sensitive launches.
Yes, completely. The License Pack grants you full ownership of the formulation. Use it with any manufacturer, in any market. No royalties, no ongoing fees.
All deliverables are provided as professional PDFs with source citations. Raw data and specifications are also available in structured formats (CSV, JSON) for integration with manufacturing systems.
We formulate across the full spectrum of supplements, nutraceuticals, vitamins, probiotics, and botanicals, including multivitamins, targeted nutrition, sports performance, beauty-from-within, metabolic health, condition-specific, and hemp-derived products.
Yes. We analyze population-specific research to ensure your formulation addresses real biological differences based on clinical research. This includes formulations optimized for specific demographics, age groups, or health conditions.
We provide documentation aligned with FDA (US), EFSA (EU), MHRA (UK), SFDA (Saudi Arabia), GSO (GCC), Health Canada, and TGA (Australia). The Global License Pack includes multi-market compliance from day one.
Every License Pack includes an Evidence Dossier: the clinical studies and scientific rationale behind every ingredient choice. This is your documentation if you face regulatory scrutiny, retailer questions, or legal challenges in any market.
The EU requires health claims to be pre-authorized by EFSA, which has rejected roughly 80% of submissions. Our Global License Pack aligns with EFSA Article 13.1 authorized claims to ensure your product can make legal claims in Europe. For novel claims, we offer Article 13.5 application support.
Yes. Our Global License Pack includes SFDA/GSO-ready documentation for Saudi Arabia and the wider Gulf region. We also provide halal-compatible ingredient guidance and Arabic label compliance support.
The Ceuvita Trust Mark is a consumer-facing verification that your product was scientifically formulated. It includes a QR code linking to a plain-language explanation of the science behind your product, building consumer confidence at shelf.
You can display the Trust Mark on product packaging, e-commerce listings, marketing materials, and retail displays. Guidelines for proper usage are included with your License Pack.
Yes. Our Manufacturing Brief is designed to be CMO-ready, with complete ingredient specifications, quantities, suggested suppliers, and process guidance. Most manufacturers can begin production immediately.
Our formulations are designed with stability in mind, using ingredient forms and combinations with established shelf-life profiles. Actual stability testing is performed by your CMO. We provide guidance on expected stability characteristics and recommended testing protocols.
We're manufacturer-agnostic. Your formulation works with any CMO you choose. We can provide recommendations if needed, but there's no requirement to use specific partners.
Our Commitment
Ceuvita exists to make pharmaceutical-grade formulation science accessible to every brand willing to hold itself to a higher standard.
Join the waitlist for early access to Ceuvita. Pharmaceutical-grade formulation science and regulatory-ready documentation, delivered in 5 to 15 days.
