Manufacturing Facility
Production at Curexa stands as the driving force of precision, performance, and purpose. Guided by our mission, we transform scientific expertise and craftsmanship into high-quality therapies that meet real-world healthcare needs. Our teams operate with unwavering passion, discipline, and innovation; ensuring that every process upholds the highest standards of quality, safety, and efficiency.
We apply advanced technology, validated processes, and qualified personnel to deliver products that meet global quality standards.
Our Formulation Capabilities
We are specialized in three cephalosporin dosage forms, each manufactured in dedicated areas to prevent cross-contamination:
- Capsules
- Dry Powder Suspensions
- Dry Powder Injections
Each production area is supported by dedicated HVAC systems, controlled personnel and material flows, and robust contamination-control protocols. All manufacturing operations are carried out on qualified equipment with validated processes. This ensures consistent product quality, uncompromised safety, and reliable therapeutic efficacy.
Technology That Sets Us Apart
At Curexa Health, our production operations leverage automation and stringent environmental controls to ensure uncompromised product quality. Fully automated lines, from vial washing and filling to sealing and labeling; maintain aseptic integrity at every stage. Our facility operates under validated sterile conditions, supported by HEPA filtration, controlled pressure differentials, and validated sterilization cycles, providing a consistently contamination-free environment.
To remain aligned with global pharmaceutical standards, we continuously upgrade our infrastructure, equipment, and processes. All aseptic manufacturing lines undergo routine Media Fill Trials (Aseptic Process Simulations) in accordance with international regulatory requirements, ensuring that every sterile batch meets the highest benchmarks for safety, sterility, and reproducibility.