Founded in 1967, our laboratory performs tests for physicians and hospitals in a wide area. Since the 1980’s, we have been performing analytical and diagnostic testing for the pharmaceutical industry. We have been offering customer-oriented full central laboratory service for phase I-IV clinical studies since the mid-1990’s. In 2014, we began offering cellular analysis and molecular diagnostic studies of samples in the pre-clinical phase according to GLP and conducting quality checks on the manufacture of active ingredients under GMP conditions.
Spranger Laboratories, an environmentally-certified facility, are accredited according to directives 93/42/EEC, 90/385/EEC, DIN EN ISO 15189 and DIN EN ISO 17025.