Eurofins Pharma Quality Control SAS

Eurofins Pharma Quality Control SAS operates as a GMP-certified laboratory with extensive experience in chemical and microbiological testing. We support the analysis of raw material, intermediates, finished sterile & non-sterile pharmaceutical products for the Human and animal health industries.
We offer a full range of testing services, including but not limited to: extensive chromatography facilities (HPLC, GC, TLC, and GC-MS), spectroscopy (UV-VIS, IR and FTlR), metals analysis via AA, GFAA and ICP-MS, packaging testing, dissolution testing and physical testing of tablets, as well as clinical logistics and microbiology services including environmental monitoring (water, gas testing). Our ICH-VICH storage capacity is one of the largest in Europe.

Our expertise spans everything from routine standardised testing to complex, tailor-made studies designed to meet your unique requirements.

We are certified in accordance with GMP (Good Manufacturing Practice) and have been accredited with DIN EN ISO 14001 for the testing. We are listed by the World Health Organization (WHO) and have been audited successfully by the FDA and EMA.

Our teams of scientists and project managers support you during the whole outsourcing process, from testing to reports. Data is accessible online 24/24: LabAccess.comSM.
In close cooperation with our Eurofins BioPharma Product Testing network of laboratories across Europe, we are able to offer the full service package, including bioassays.
Our local presence ensures personalised customer support for all analytical needs.