CDMO SERVICES FOR STERILE AND NON-STERILE LIQUID SOLUTIONS & SUSPENSIONS
Comprehensive CDMO services for sterile and non-sterile liquid solutions and suspensions backed by an experienced team and state-of-the-art facilities across the globe.
TriRx is committed to providing comprehensive pharma CDMO solutions, from development through to packaging and distribution, ensuring quality and reliability at every step of the manufacturing process. We excel in both sterile and non-sterile pharmaceutical manufacturing for liquid solutions and suspensions, leveraging our expertise across multiple global facilities. Utilizing sophisticated clean-in-place (CIP) and sterilization-in-place (SIP) technologies for the highest standards of product safety and compliance, we can support a broad spectrum of healthcare products, including those for both human and animal health, maintaining an excellent record of compliance and operational excellence.
STERILE/NON-STERILE LIQUIDS DEVELOPMENT & ANALYTICS
Our robust development and testing capabilities underscore our commitment to innovation and quality. Our teams leverage cutting-edge technology and deep industry knowledge to ensure the development and testing of sterile and non-sterile liquids meet the highest standards. From formulation development to analytical testing and stability studies, we provide comprehensive support to optimize product efficacy and safety.
STERILE/NON-STERILE LIQUIDS MANUFACTURING
Our liquid manufacturing capabilities are a testament to our versatility and commitment to excellence. We offer extensive services in sterile and non-sterile liquid manufacturing, including aseptic liquid filling, terminal sterilization, and comprehensive handling of solutions, suspensions, and colloidal dispersions. Our facilities are designed to accommodate a wide range of product types and packaging requirements, ensuring flexibility and efficiency from small batches to large-scale commercial production.
Sterile Pharmaceutical Manufacturing
Specializing in aseptic compounding, aseptic liquid filling, and packaging of sterile injectables, ointments, suspensions, solutions, and emulsions, our facilities use Clean-in-Place (CIP) and Sterilization-in-Place (SIP) techniques to ensure the highest standards of product sterility.
Non-Sterile Pharmaceutical Manufacturing
With capabilities to produce large-scale batches of non-sterile liquids, solutions, suspensions, and colloidal dispersions, we are well-positioned to ensure consistent quality and stability in manufacturing for a variety of non-sterile drug products.
STERILE/NON-STERILE LIQUIDS PACKAGING
We provide innovative packaging solutions for sterile and non-sterile liquids tailored to client needs and regulatory requirements. Our packaging lines are fully integrated and serialized, capable of handling a variety of formats, from vials and bottles to complex custom configurations, ensuring product integrity and patient safety.
Our sterile and non-sterile services take place in our facilities in Segré, Speke, Huntsville, and Shawnee, with each location offering unique capabilities. Our Huntsville facility specializes in large-scale production of solutions, suspensions, and other non-sterile formats in a space combining development, manufacturing, packaging, and warehousing. Shawnee and Segré specialize in high-volume sterile injectable manufacturing for both solutions and suspensions. Speke offers robust capabilities, including non-sterile liquid filling, as part of its wide biotech and human health manufacturing services.