Our Products
Flexible, agile, and proactive laboratory services dedicated to global clinical development
Hardware certification
The device and the COVID-19 IgG / IgM immunofluorescence rapid test & antigen are certified by TÜV SÜD, CE and comply with IVD regulations according to Directive 98/79 / EC, and meet all applicable quality standards for in-vitro diagnostics. A pharma code for the product is available.
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In Switzerland, we are the only dealer of innovative devices. Become our partner and discover the many advantages with which your company can grow.