By end of 1998, the first European quality and safety requirements for in vitro diagnostic medical devices, the European Directive 98/79/EC (IVDD), stepped into effect. After almost 20 years in
HSE•AG draws on its unique experience gained from developing automated systems for a diverse range of workflows in life science and molecular diagnostics. Based on this extensive knowledge, we understand the challenges of your workflow and how to overcome them. HSE•AG has a broad spectrum of OEM modules that act as building blocks when developing new automated solutions. They can be easily customized for use in your automated workflow reducing the time-to-market and risk in your project.
Our OEM Modules
Touch base with us
Whether you are looking for new technical approaches to automate laboratory workflows, you need to ensure regulatory compliance of your product, or you want to reduce costs and shorten the time-to-market, we have the tools to ensure your business growth. We specialize in turning ideas into cutting-edge solutions, so simply contact us and tap into our technology and application knowledge.
Diagnostic system development projects can be more prone to failure than you would think. Despite the eye-watering amounts of time and money that flow into these projects, relatively simple aspects
Without partnerships I would have hardly ever had success — but I had to learn that from experience.
by Thomas Hanselmann This blog post reviews a must-read paper for anyone involved in next-generation sequencing (NGS) – “Short Barcodes for Next Generation Sequencing” by Mir et al. (2013) –
by Thomas Hanselmann An Example of Fluidic Pressure Data from a DNA Sequencing Machine using simple PCA & Clustering.