The Single-Roof Method, mapped
Seven places a supplement can go wrong. You can check all seven.
Pharmacist, designer, regulatory and QC sit in the same building, on the same payroll. There are no vendor handoffs to blame, no plant we have never visited, and no deadline from a client that could push a batch out the door before it is ready.
Step by step
From an empty bench to a released batch.
The brief comes from us
A product starts with a gap our own team can defend: an active worth taking, a dose that is actually effective, a market we can supply legally. Nobody hands us a brief and a deadline.
Formula development
Our pharmacists and food technologists set the actives, the dose and the form, then argue it out with our regulatory team before a single kilo is ordered.
Raw materials, bought and re-tested
Actives are sourced on specification rather than on price. Every delivery is quarantined and re-tested in our own laboratory: identity, actives, contaminants. If it misses the claim, it goes back to the supplier.
Design & packaging
Our design team prepares the label, the box and the dossier artwork, checked line by line against the labeling rules of every market the product will ship to.
Production
Manufacturing in an ISO/GMP environment: mixing, forming, filling and packaging, every step documented and signed. Tablets, capsules, powders and creams on parallel lines.
Quality control
Microbiological and physicochemical analyses, dissolution testing, weight, appearance and labeling checks, plus an independent third-party panel, before any batch is released.
Release & dispatch
A batch ships only once both laboratories have cleared it. Palletizing, export documentation for the EU and the U.S., and a Certificate of Analysis filed against the batch number printed on the bottle.
Quality assurance
Every batch goes through the same control.
Our laboratory and procedures are aligned with ISO 22000 and ISO 22716 standards. This means traceability of every raw material, every batch and every finished product.
- Incoming raw material inspection
- Microbiological analysis
- Physicochemical analysis
- Independent third-party lab testing, accredited per market
- Certificate of Analysis for every batch
- Stability studies
- Batch-to-batch traceability