Designing a robust lateral flow test specification for high-volume manufacture
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How to: improve lateral flow test output while focusing on core business activities
How to: reach new markets with a lateral flow contract manufacturing services provider
Cost and supply benefits when partnering with a lateral flow test contract manufacturer
The importance of lateral flow for decentralised molecular testing
The COVID-19 pandemic has seen the global mobilisation of diagnostics: predominantly lateral flow rapid tests and lab-based molecular tests. The deployment of laboratory molecular testing has highlighted the barriers in reaching the widest patient cohort and delivering test results as fast as possible. Abingdon Health spoke with… Read More
Accuracy and Flexibility: Using lateral flow in the rapid deployment of PCR and RPA
COVID-19 increased the need to deploy novel diagnostics in great numbers and quickly. Companies mobilised capabilities and capacities to ensure those in most need have access to testing solutions. Everyone has now heard of PCR’s (Polymerase Chain Reaction) ability to copy and amplify specific nucleic acid sequences. This revolutionised molecular… Read More
COVID-19 lateral flow rapid tests: developers need to consider scale-up from the start
Learn the crucial reasons why scale-up should be considered early in the assay development process. Read More
Second source lateral flow manufacturing
Aiding supply and demand in potential disruptive periods such as the current COVID-19 outbreak. Read More
Be IVDR ready to protect your assay and business
Learn about the key changes to the In Vitro Diagnostic Directive and the areas you should be actively considering. Read More
Selecting antibodies for lateral flow assays
Learn about some of the technical considerations for selecting antibodies during lateral flow assay development. Read More
What is needed to initiate lateral flow development?
Nina Garrett, Head of Assay Development, looks at the technical considerations when starting a lateral flow project. Read More
Grasp ‘Software as a Medical Device’ regulation for success in the US mHealth market
mHealth Software Regulation: part II: Regulations for mHealth in the USA, the largest diagnostic market. Read More
