The company has more than 600 squaremeters of R&D, QC and GLP laboratories. All laboratories are BSL 2 or 3** classified and have been built to satisfy the stringent demands of the biotechnology industry.

Our 500 squaremeters GMP facility consists of 9 clean room suites of class A/B (class 100) and one suite of class C (class 10.000). All suites are equipped with state-of-the-art apparatus and are classified as BSL 2 or 3** which also allows the handling of infectious material such as HIV positive cells.
In early 2003, the existing manufacturing licence (from 1999) was extended to cover the new clean room production facility by the local government authorities.
Within this multi-purpose manufacturing facility, EUFETS is able to produce a variety of clinical trial materials in parallel according to our customers’ needs while ensuring the highest quality standards.