Euroimmun’s commitment is to deliver the highest-quality products, backed by unsurpassed scientific and technical support. EUROIMMUN US, Inc. is an FDA-registered facility and has a Quality Management System certified in conformity with ISO 13485:2016, 21 CFR 820, 21 CFR 803, 21 CFR 806, and 21 CFR 807 (A to D) by Intertek. EUROIMMUN US, Inc. has obtained a significant number of product clearances from the FDA, with the majority of products also carrying CE marking.
Our areas of expertise are supported by a strong scientific team committed to improving healthcare by delivering innovative, clinically relevant diagnostic assays, and automation that aid in the diagnosis of autoimmune and infectious diseases. Worldwide, Euroimmun offers one of the most extensive test menus in a variety of technology platforms:
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