Applications by Process
Fluid handling and freeze/thaw management in biomanufacturing
From downstream processing to fill & finish, fluid handling, freeze-thaw and cold storage operations play a critical role in protecting valuable drug substances. Single Use Support provides solutions for aseptic filling, freezing, thawing, storage, and transport that help streamline biomanufacturing workflows while reducing contamination risks and product loss.
Built on standardized yet flexible single-use technologies, our solutions support the safe handling of APIs (active pharmaceutical ingredients), buffers, media, biojoncugates, vaccines, cells, and other high-value biopharmaceutical products across manufacturing and logistics operations.
Seed Train Intensification
Safe aliquotation, freezing, storage, and handling of high-density CHO cells as part of upstream bioprocessing process intensification with minimized contamination risk and maximum process efficiency.
Fermentation
Cold Chain Handling for Microbial, Bacterial & Mammalian Fermentation. For improved fermentation production, manufacturing suites must be equipped with scalable, cost-effective and robust process solutions for large volumes up to hundreds of liters per batch.
Fill & Filtration
In biopharmaceutical manufacturing, fill-filtration is a critical process step. To ensure product quality and regulatory compliance, bioprocess fluids must be filtered, filled, and aliquoted with a high degree of accuracy and consistency. Single Use Support helps manufacturers overcome these challenges through automated, GMP-ready fill-filtration solutions.
Freeze & Thaw
Freezing and thawing processes enable the safe storage, transport, and management of valuable drug substances throughout the cold chain. Single Use Support provides advanced freeze-thaw solutions designed to ensure controlled, reproducible, and scalable cold chain operations.
Freeze & ULT Storage
Integrating harmonized freezers can make cold chain operations, from controlled freezing to ultra-low temperature storage of bulk drug substances, more efficient. This can be achieved even within existing facilities, resulting in fewer manual handling steps and higher capacity and scalability.