Company Description & Background
With a proven track record of providing quality scientific solutions for the largest pharmaceutical and biopharmaceutical companies in the world, Eurofins Lancaster Laboratories is a global leader in bio/pharmaceutical laboratory services providing comprehensive, innovative and timely solutions to streamline all of your CMC testing requirements.
A member of the Eurofins BioPharma Product Testing Group, Eurofins Lancaster Laboratories has a global capacity of more than 500,000 square feet within our locations in the U.S. and Europe. All of our facilities offer cGMP-compliant laboratory services and operate under the same strict quality control program. Utilizing the same LIMS system and centralized billing, working with any of our global facilities is a seamless operation. We also provide secure 24-hour data access via
LabAccess.comSM
. Markets Served
We provide full CMC testing services to support more than 1,000 virtual and large bio/pharmaceutical companies and CMOs.
Services & Capabilities We provide the flexibility to manage your drug development programs more efficiently through your choice of five unique service models, including the award-winning Professional Scientific StaffingSM
www.LancasterLabsPharm.com
Eurofins Lancaster Laboratories, Inc. 2425 New Holland Pike PO Box 12425 Lancaster, PA 17605-2425 Tel: 717-656-2300
(PSS), as well as Full Time
Equivalent (FTE) and Managed Hours programs. You can choose the best, most cost-effective service solution for your project goals at any of our global facilities. Our breadth of services include: • Method development, optimization, cGMP qualification and validation • Drug substance and product characterization • Full stability and release programs for clinical and marketed products • Raw material and excipient testing (USP/NF, EP, JP) • Microbiology services including mycoplasma, rapid mycoplasma, sterility, endotoxin and particulate matter testing
• EU release testing • R&D and cGMP cell banking and storage • Viral and molecular biology testing • Process/facilities validation – viral clearance, residual impurity testing, extractables & leachables, water testing, environmental monitoring, disinfectant efficacy, on-site sample collection • Consulting/protocol writing.
www.americanpharmaceuticalreview.com | | 17
EUROFINS LANCASTER LABORATORIES, INC.
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