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Introduces new modular sterile filling system at its facility in Wasserburg, Germany.
February 6, 2025
By: Charlie Sternberg
Recipharm’s new modular sterile filling system, specifically tailored for process development, pilot scale and clinical supply, is now fully operational at its facility in Wasserburg, Germany. This advanced system performs aseptic filling within a Grade A isolator and operates in full compliance with GMP standards.
The system features interchangeable modules that support various product types, such as syringes and vials. An additional pre-filled syringe (PFS) module is being added to the installation, broadening the system’s capabilities and cementing its position as a versatile and reliable solution for pharmaceutical and biotech companies alike.
The line can deliver 500 to 50,000 units per batch, covering all the development phases of a product. In addition, the system provides great efficiencies and cost saving by limiting the loss of high-value products to less than 500mL and preserving material for clinical trials.
This new unit complements Recipharm’s existing development and commercial filling capabilities. Unlike traditional large-scale production systems, the unit is optimized for small-batch production, offering a fast and flexible solution for clinical development projects across rare disease pharmaceuticals, cell and gene therapies, and other advanced and emerging modalities with highly focused patient populations. This also makes it an ideal companion to ReciBioPharm’s Biologics and ATMP services. Additionally, when used with Recipharm’s ReciPredict, the product benefits from optimized time and cost efficiency, supporting a seamless tech transfer to commercial production.
Gregor Kawaletz, Chief Commercial Officer, Recipharm, said: “With this unit, we offer our clients a flexible, high-quality and GMP-compliant solution for their development and clinical production needs. This installation reflects our commitment to investing in innovative technologies that enable faster and more efficient pharmaceutical development.”
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