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Performance verification is the stage at which a lateral flow assay moves from development understanding to formal analytical evidence. This article explains how intended use and design inputs shape verification strategy, how CLSI-guided studies are structured, and why robust documentation is critical for transfer, submission, and product readiness.

Moya joins us at an exciting stage for our Lateral Flow Development services. Moya brings over 15 years’ experience in Lateral Flow Assay development and a reputation for excellence in the field, with technical lab expertise, project management skills, and proven leadership. She has a strong track record of taking assays from development through to manufacturing, across multiple sectors, assay types and deployment settings. In her new role she will lead projects from feasibi

Fleet Bioprocessing launches contract lateral flow device development, offering end-to-end LFD feasibility, optimisation, verification and validation services.