Symbiosis Completes Qualification of New FDP 50 Flexicon Automated Fill/Finish Line 

Symbiosis Pharmaceutical Services, a global contract manufacturing organization (CMO) specializing in the sterile manufacture of injectable drug products, has successfully completed qualification of its new FPD 50 Flexicon automated fill/finish line at its new commercial production facility in Stirling, Scotland. 

The fully integrated sterile liquid fill/finish system operates under a Grade A Restricted Access Barrier System (RABS). Designed to deliver with both precision and efficiency, it incorporates rapid transfer ports for aseptic handling and high-accuracy vial filling with flexicon pump technology. The system also features a rotary crimp mechanism to ensure consistent overseal application and secure closure. 

Colin MacKay, CEO of Symbiosis, said: “The qualification of our automated fill/finish line is a major step forward for Symbiosis. It enhances our technical capabilities and expands our capacity at a time when demand for high-quality sterile manufacturing continues to grow. Most importantly, it strengthens our ability to help clients bring vital therapies to patients quickly and to the highest regulatory standards.” 

Symbiosis will commence commercial production at their new facility in Q4 2025, manufacturing batches of up to 15,000 vials, and representing the latest in a series of recent milestones for the company.