When products touch patients, quality is non-negotiable. Our facility, systems and people are being built to protect health at every step of production.
The facility is being developed on a total area of over 13,000 m², with a planned built-up factory area of over 4,000 m² and a GMP-compliant layout that provides independent zones for each production stage.
Each stage in a dedicated zone ensures smooth workflow, quality control and prevention of cross-contamination.
Molding, injection & assembly lines
ISO 7 – ISO 8
Central EO sterilisation
Sterile filling & labelling
Material & product stores
Testing & QC
Administrative offices
Support & utility systems
The factory is being equipped with an integrated suite of modern machinery across all manufacturing stages.
Designed for precise component moulding using approved medical materials.
For producing medical tubing and lines with consistent quality.
Secure, safe bonding without additional adhesives.
Integrated assembly lines for finished products.
For validated sterilisation to ensure product safety.
Leak testing and quality assurance before release.
We are committed to manufacturing in accordance with recognised international frameworks and are preparing full documentation for regulatory registration.
Good Manufacturing Practice
Medical device quality management
Sterile product packaging
Preparing for registration & accreditation
These are targeted standards — certification is in progress. We will obtain each accreditation progressively as the project advances and the product portfolio grows.
Raw materials verified and tested against specification before use.
Continuous monitoring throughout cleanroom production.
Validated ethylene-oxide processes with sterility assurance.
Finished-product testing and documented batch release.
The facility is currently under construction. We'd be glad to connect with you to discuss your medical-supply needs and explore future collaboration.