Eurofins PHAST GmbH in brief

With its two business units, laboratory services for the development of human and veterinary pharmaceuticals and laboratory supply with the daily analytical requirements for Reference Standards, Eurofins PHAST GmbH makes a significant contribution to increasing patient safety.

To this end, Eurofins PHAST GmbH is taking on challenging tasks for its customers in the international pharmaceutical industry with growing success: In addition to efficacy and safety, the quality of a pharmaceutical drug is of central importance for the patient. In order to ensure the highest possible quality of medicines, there are correspondingly strict legal framework conditions for their development, manufacture and control. All related activities are strictly controlled and comprehensively documented. The resulting costs for research-based pharmaceutical and biotech companies are enormous. This applies in particular to the labor-intensive and time-consuming development of pharmaceutical drugs. With its comprehensive range of services, Eurofins PHAST GmbH is an internationally sought-after service company for precisely this purpose.

High-quality reference materials are required for the qualification of laboratory equipment, the calibration and validation of analytical methods and for quality control in daily routine analysis. In order to save time and costs, pharmaceutical laboratories use pharmacopoeia standards, e.g. USP or EP/EDQM, which have an official status and do not have to be recognized separately by the respective regulatory authorities when used in accordance with the pharmacopoeia. Eurofins PHAST GmbH offers the international pharmaceutical industry USP and EP/EDQM Reference Standards in the form of chemical substances and biological preparations for pharmacopoeia-compliant analyses online in the webshop www.reference-standards.com.

As a “USP Authorized Distributor”, Eurofins PHAST GmbH is the official distributor in Europe for Reference Standards of the United States Pharmacopeia.

Your laboratory service benefits at a glance:

• Our laboratories - key to shortening time to market: manufacturing authorization, GMP, central contact for quality control, manufacturing, qualified persons (QP), inspections by EU and US authorities, BSL 2 regulatory authorization, import, EU retesting.
• Combination of state-of-the-art analysis technology with highly qualified technical expertise, permanent expansion of the range of services ... flexible in technology - experience - knowledge - capacity

Eurofins PHAST laboratories are part of the Eurofins BioPharma Product Testing laboratory network in Germany. Further information at www.eurofins.de/biopharma

At www.eurofins.de/phast you can directly access the laboratory services of Eurofins PHAST GmbH.