Advancing Therapeutics Through Biotechnology Excellence
Specializing in recombinant protein production, API manufacturing, and sterile filling across vials, ampoules, and prefilled syringes. Partner with us for world-class pharma solutions.
Facility Campus
The Synvion campus operates multiple high-capacity sterile manufacturing lines for liquid, lyophilized, and injectable dosage forms. Our world-class infrastructure is designed to meet the most rigorous international standards, including WHO-GMP and EU-GMP compliance.
API PRODUCTION UNITS
4 units total 2,600 m²
LYOPHILIZATION (FREEZE DRYING)
22 m² Capacity: up to 80,000 vials (2R format)
ANALYTICAL LABS
ISO-classified cleanrooms (ISO-5 / Grade A for critical aseptic zones)
TOTAL FACILITY AREA
15,000 m²
Manufacturing in ISO-Certified Environment
Products are manufactured in ISO-certified facilities operating under PIC/S GMP and EU regulatory frameworks, with inspections conducted at appropriate intervals.
- Automated Sterile Filling Lines
- Grade A Cleanroom Environments
- Stability Testing Chambers
- Advanced Quality Control Labs
Automated Filling Lines
Our filling lines utilize the latest European isolator technology, minimizing human intervention and ensuring the highest level of sterility for our vials and syringes.
Quality Control Center
Our on-site laboratories are equipped with HPLC, mass spectrometry, and biological assay systems to perform real-time release testing and stability monitoring.
