MANUFACTURING · CDMO INDUSTRIAL PRODUCTION
Integrated manufacturing.
Force One: 8,000 m² of production in Sousse, Tunisia. Qualified cleanrooms, injection moulding, automated assembly, sterilization and packaging, all managed in-house.
INTEGRATED INDUSTRIAL CAMPUS
Force One connects capacity, quality, and execution.
Our Tunisian site concentrates critical series-production operations in a pilot environment, so we can move fast without losing documentation control or quality discipline.
4,000m²
Building footprint
700 m²
ISO 7 cleanroom
100%
Qualified partnerships
What the site delivers right away
Legible capacity
Available industrial resources, constraints, and ramp-up rhythms are visible from the scoping stage.
Built-in quality
Cleanrooms, line qualification, and traceability are built into daily production.
Direct dialogue
Production, quality, and industrialization teams work from the same data and priorities.
« Force One embodies operational proximity: your audits, your pace constraints, and your quality requirements become our production routine. »
Mohamed Rekik, Managing Director
PRODUCTION FLOW
Three areas of expertise, one controlled chain.
01 · MOULDING
Injecting with precision and repeatability
Micro-moulding, multi-material and technical polymers are managed to hold dimensions, pace, and product stability. Injection machines from 10T to 320T, tooling design and management, FAT/SAT/IQ/OQ/PQ, lot sizes from 100 to 1 million parts, overmoulding, thermoplastics and silicone.
02 · ASSEMBLY
Combining automation and expert craft
Automated lines and qualified manual stations combine according to volume, complexity, and required control level. Solvent bonding, ultrasonic and high-frequency welding, UV adhesive bonding, pad printing, overmoulding, catheter forming, PVC/EVA pouch fabrication, 3D printing.
03 · STERILIZATION
Securing sterility through to packaging
EtO, gamma, beta (e-beam), X-ray irradiation and sterile packaging are selected and validated according to the device and its lifecycle, following ISO 11135 and ISO 11137.
Unit traceability
From component to delivered lot, every step stays documented and usable.
Cycle validation
Critical parameters are qualified, monitored, and reviewed with the quality teams.
Series scale-up readiness
The transfer to target pace happens with clear visibility on risks and capacity.
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One device. One vision.
One partner.
Let’s talk about your project: design, manufacturing, compliance. Our team responds within 24 business hours.