Frontage Europe Has Relocated Its Bioanalytical Laboratory and Further Expands Its Capabilities
The bioanalytical laboratory is the forefront in our services portfolio. It features state-of-the-art equipment for quantitative mass spectrometry, ligand-binding and biomarker assays. The platforms, including LC-MS/MS,
The laboratory operates under Good Laboratory Practice (GLP) quality system and complies with Good Clinical Practice (GCP) to support clinical studies. Bioanalytical assay validation and sample analysis are performed in compliance with the international ICH M10 regulatory guidance. Expertise on pharmacokinetics and scientific advice on the preparation of regulatory documents (e.g. IB, IND) are our added value.
To meet clients' demands,
We also offer custom synthesis services of radiolabeled (14C, 3H, 35S) and stable-labeled (2H, 13C, 15N) compounds. Our dedicated team can help you understand the metabolism of your compound by high resolution mass spectrometry analysis (Q-Exactive Orbitrap) of in-vitro matrices (e.g. microsomal, hepatocyte incubations) and in-vivo samples from preclinical and clinical studies.
If you are interested in learning more about our capabilities, please contact us at sales@frontagelab.com.
About Frontage
Frontage operates 26 sites worldwide and has played a pivotal role in helping clients secure regulatory approvals across the US, Canada, Europe, and Asia.
For more information, visit www.frontagelab.com.
Media Contact:
xniu@frontagelab.com
(610) 232-0100
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