In this post, we’ll go over three key aspects that ensure lateral flow dispensing equipment is made to market standards. We have all the basic steps mentioned that will guide you throughout your journey.
Overview of lateral flow assay equipment
In resource-constrained or non-laboratory contexts, lateral flow assay equipment is now utilized for qualitative, semiquantitative, and quantitative monitoring. In biomedical, phytosanitary, veterinary, feed/food, and environmental contexts, testing on pathogens, medicines, hormones, and metabolites are performed.
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Get the fundamentals right.
Effective label and antibody conjugation, as well as the selection and application of the appropriate reagents, nitrocellulose membranes, and absorption pads, are all required for successful production of lateral flow assay equipment.
Then they are put together in a lateral flow immunoassay (LFIA), ensuring they all interact to give the required result as stated in the assay and market requirements.
Lateral flow dispensing equipment works on a few basic principles. However, it requires time, planning, and a rigorous research and production strategy to reach to the point where the test is suitable for commercial usage.
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Scaling-up a Successful Assay
The next critical stage is to transform a test from a prototype to a market-ready product. It’s crucial to make batches of increasing sizes at this time to confirm and verify that the scaled-up version of the lateral flow assay equipment fulfils the intended assay and market criteria.
The assay development team can compare scaled-up requirements to performance by manufacturing in increasing batch sizes.
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Automation elation
Automation guarantees that lateral flow assay equipment is designed and manufactured to consistently deliver correct results with high inter- and intra-batch repeatability.
However, investing in cutting-edge automated technology has a price tag. When commissioning assay research and manufacture, there is no need to spend money on equipment and subsequent staff.
The time saved by not having to build the lateral flow dispensing equipment, train workers, or incorporate its use into normal operating procedures allows a client to focus on commercializing an assay.
Customer Driven development
Customer-driven development and manufacture of lateral flow assay equipment is the most important aspect. You will have access to a cost-effective final Immunoassay product through the best company that meets all of your requirements.
Some of the requirements include limit of detection, diagnostic and analytical specificity and sensitivity, reproducibility (inter-lot, inter-day, inter-lab), and quality control definition.
The experimental process entails optimizing a variety of input factors that have a direct impact on the quality of the end result, which is described by output variables.
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Bottom Line
In the end, having efficient lateral flow assay equipment and the appropriate production resources results in the best product being produced. However, there are two aspects that are required to tie all of the above together: knowledge and experience.
Expertise ensures that lateral flow dispensing equipment is optimised and scaled-up efficiently for routine manufacturing, while experience ensures that tried and true methods and procedures are used, regulatory issues are considered, and market needs are created and followed.
