Facilities designed to meet pharmaceutical and cosmetic requirements
4,500 m² dedicated to production, with classified areas and segregated flows to ensure compliance with GMP, ISO 22716, and ISO 13485 standards.
An auditable and secure industrial site
Surface area & capacity
4,500 m² of surface area, 4 production zones, 2 units dedicated to ISO 13485, and one unidirectional flow line.
Controlled environment
ISO 8/9 cleanrooms, continuous monitoring of parameters (temperature/humidity/pressure), HEPA filtration systems.
Logistics & storage
Separate receiving and shipping areas, controlled storage of raw materials and finished products, FIFO traceability.
Maintenance & safety
Planned preventive maintenance, integrated HSE system, and business continuity plans to ensure on-time delivery for our clients.
Flow management quality
Segregated material and personnel flows to minimize cross-contamination risks and ensure batch integrity.
Digital traceability
ERP integrated with the serialization system, badge-based tracking, and electronic audits. Batch history accessible in just three clicks.
Human scale
Qualified team trained in GMP, EPS, and HACCP. A QSE coordinator is present at each batch start-up.
Our industrial capabilities in figures
Our packaging expertise
A versatile industrial setup covering the entire packaging chain, from primary packaging to shipment.
Detailed technical dossier
Throughput, formats, specifications: receive our complete dossier upon request.
Request the dossierSite visit or industrial project?
We respond within 48 hours and organize capacity audits.