Our global sterile filtered liquid capabilities are designed to enhance and streamline your process, from clinical-phase trials all the way through to commercial production:
As a trusted partner, we bring together products and services from across our company to offer the industry’s highest quality sterile filtered liquid capabilities for the biopharmaceutical industry. All manufacturing locations operate according to
ISO 9001:2015 and GMP principles, so we can address your global needs and provide faster turnaround for your order.
Process steps such as media and buffer preparation or hydration of bulk powders can consume precious time, labor, and manufacturing floor space. Our ready-to-use sterile filtered liquid solutions eliminate the extra tasks, workforce and space associated with hydrating bulk powders, such as tubing and refilling, sample taking, and additional quality control testing streamline your processes while providing advantages such as:
Your sterile filtered liquid arrives ready-to-use in the quantities you need, with no waste and no excess to inventory. Our manufacturing facilities are specifically designed to provide sterile filtered products in a wide range of final vessel formats, from standard PET bottles to standard or custom bags, as well as custom volumes and formats. Our products are sterile filtered liquids which are supporting your research and further manufacturing processes. To ensure safe delivery of your sterile filtered liquids, our packaging and transport options include:
Water for injection is the key starting ingredient for all our liquid products. We ensure consistency, security, and EP and USP compliance by establishing redundant water for injection (WFI) supplies at all our facilities. This bulk-packaged water is suitable for the preparation of both upstream and downstream process solutions in industrial and regulated bioprocessing applications.
All our liquid media facilities worldwide are part of our comprehensive Global Quality Management System, assuring the highest product consistency, reproducibility, performance, and expertise. We are committed to meeting or exceeding all relevant international guidelines and regulations, and we maintain quality certification programs at all facilities with on-site quality control testing. Our Global Quality Management System is certified as ISO 9001:2015, and all sites voluntarily comply with the Joint IPEC-PQG Guide on Good Manufacturing Practices (GMP) for Excipients and applicable sections of Annex 1 of the EU Guidelines to Good Manufacturing Practice for Medicinal Products.
To provide a consistent supply of material for your business continuity, our Global Raw Material Management Program is robust, controlled, and coordinated to ensure that our incoming supply is safe and secure. We also:
To help you stay on top of regulatory changes and simplify your processes, our manufacturing sites have 100% access to our industry-leading Emprove® Program. This powerful, always up-to-date repository of current and anticipated regulatory data supports our high-quality pharmaceutical and biopharmaceutical raw materials and consumables, providing you with comprehensive documentation that can:
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