At Abingdon Health we work with companies who have outgrown in-house production capacity or need to transfer their assay to a larger manufacturer.
We provide high-volume lateral flow manufacturing services to ISO13485 and GMP quality standards to enable our customers to take the next step in increasing their market share.
During the scale-up process, we take assays through a series of validation and optimisation steps.
Design specifications are configured for increased batch size production where a pilot batch will be tested to cross-reference assay performance. Then, validation batches of increasing size will be produced on our automated equipment to ensure design specifications are robust enough to cope with the rigours of routine lateral flow manufacture.
Once an assay passes into routine manufacture the use of our state-of-the-art automated equipment helps to provide customers with optimal batch sizes in a time-efficient and cost-effective manner.
Contact us today on +44(0) 1904 406082 or at email@example.com to see how we can help you achieve your market ambitions.
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