Eurofins│PHAST at a Glance
Eurofins | PHAST is part of the Eurofins BioPharma Product Testing Group in Germany and supports the international pharmaceutical and biotech research companies in drug development.
The Eurofins | PHAST “Centers of Excellence” are established for spectroscopy, dissolution/drug release, and solid-state analytics. Clinically relevant dissolution methods are developed and validated, and the in vitro performance of dosage forms is characterized. Beyond this, the Eurofins | PHAST expertise extends to particle characterization and molecular structure elucidation.
Being a “USP Authorized Distributor”, Eurofins | PHAST is official source for reference standards of the United States Pharmacopeia in Europe.
The highly qualified staff of Eurofins | PHAST allows maximum flexibility and quality. All laboratories have been successfully GMP-certified at international level. Multiple FDA inspections are an additional confirmation of the consistently high quality level of Eurofins | PHAST.
- Our labs – key to shorten time to market: manufacturing license, import license, GMP, EU-retest, batch release testing for clinical studies and/or market supply, QP-service, inspected by EU and US, BSL 2 licence
- Combination of state of the art analytical technologies with highly specific technical expertise, permanently expanding spectrum … flexible in technology – experience – knowledge – capacity
Eurofins | PHAST provides the services from its sites in Homburg, Konstanz, and Frick (CH), and offers more than 6,000 m² of laboratory space. Pushing the www.eurofins.de/reference-standards button you will be guided directly to the Eurofins | PHAST services for Reference Standards.