The Single-Roof Method, mapped
30 days, not six months. Here are the seven steps that make it possible.
Pharmacist, designer, regulatory and QC all in the same building. No vendor handoffs, no "waiting on the printer," no email threads that go dark for a week. We guide you from first inquiry to finished product on your customer's shelf, in days, not quarters.
Consultation
You send an inquiry, we book a free consultation (online or at our facility) where we analyze your idea, target group and market.
Formula development
Our pharmacists propose ingredients, dosages and form. You can choose an existing formulation or create a new one from scratch.
Quote & contract
You receive a detailed quote with unit price, MOQ, lead time and packaging options. Once approved, we sign the contract.
Design & packaging
Our design team prepares the label, box and marketing materials. If you already have a brand identity, we adapt it to legislative requirements.
Production
Manufacturing in an ISO/GMP environment, raw material control, mixing, forming, filling and packaging. Every step documented. Capsules, powders and creams on parallel lines.
Quality control
Microbiological and physicochemical analyses, dissolution testing, weight, appearance and labeling checks, before each batch is released.
Delivery
Palletizing per your requirements and shipping, directly to your warehouse or distribution network. EU + U.S. compliant export documentation.
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
- Third-party lab testing (EU/U.S. labs per target market)
- Certificate of Analysis for every batch
- Stability studies
- Batch-to-batch traceability
