Get to know our
Facilities

BrownBiology Laboratory is a US-based CRO comprising cutting-edge facilities with 14 laboratory departments, 240 highly trained experts, and 5,000 m虏 worth of laboratory space and top-of-the-line instruments.

Our Laboratories

Our GMP/GLP-certified bioanalytical and CMC services are carried out by specialized teams in our dedicated laboratories across the United States.

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Analytical Development and Validation
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Bioanalysis of Small Molecules
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Bioanalysis of Large Molecules
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Bioanalysis of Oligonucleotides
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Quality Control of Small Molecules
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Quality Control of Large Molecules
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Elemental Analysis
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Microbiology
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Stabilities
10
Quality Assurance

In addition to our main laboratories, we are equipped with adjacent facilities for weighting, sample preparation and processing; a combined 100m鲁 of SCADA-monitored sample storage chambers under all ICH climatic conditions including standard and IVb zones, back-up room, refrigerated conditions, -20潞C freezers and -80潞C ultra-freezers; a microbiology cleanroom for aseptic testing and sample preparation; a containment room for work under O.E.L. Category 4 with high-potency drugs such as hormones, antibiotics or cytotoxins; a radioactivity laboratory to work with Iodine-125; purified water and technical-gas plants; emergency power generators; a fireproof data center for communication and software servers, data storage and back-up systems; as well as offices, meeting rooms, cafeteria and general facilities.

Technology

Our Cutting-Edge Expertise

Our facilities are equipped with advanced instruments, innovative techniques, and a rigorous methodology to ensure precision, compliance, and efficiency in every analytical process.

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Instruments

We are equipped with state-of-the-art instrumentation to ensure the highest accuracy and reliability in our analyses. Our laboratories feature advanced LC-MS/MS, HRMS, ICP-MS, qPCR, and ELISA platforms, as well as specialized systems for chromatography, spectrometry, electrophoresis, and immunoassays, among others. With cutting-edge automation and digital integration via LIMS, we guarantee precise, reproducible, and regulatory-compliant results for every project.

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Techniques

We employ a broad range of analytical techniques to support pharmaceutical development, from early-stage research to commercial batch release. Our expertise includes mass spectrometry, ligand-binding assays, electrophoretic separations, and cell-based bioassays, among others. With a strong focus on regulatory compliance, we develop, validate, and apply industry-leading methods to ensure the integrity and quality of your drug development pipeline.

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Methodology

Our methodology is designed to optimize efficiency and compliance across all phases of pharmaceutical analysis. We follow a structured approach, starting with feasibility assessments and method development, followed by rigorous validation and routine analysis under GLP/GMP conditions. Our team ensures that every project is executed with precision, using robust quality systems and advanced digital tools for data integrity and traceability.

Equipment

Our Platforms & Equipment

All our laboratories feature state-of-the-art instrumentation to ensure precise and reliable analysis for our clients.

Mass Spectrometry

  • AB SCIEX LC-MS/MS API 3.200 (1), 4.000 (6), 5.500 Qtrap (2), 6.500 Plus (2) and 6.500 Plus QTRAP (1)
  • Qtof Xevo G2-S with BiopharmaLynx and MaxEnt mass spectrometer
  • ICP/MS Agilent 7.700 and 7.800 (2) and digestion system Milestone Ultrawave (2)
  • LC-MS/MS Infinity with MS 6491 Agilent (2)
  • GC-MS Agilent
  • Orbitrap Exploris鈩?120 Mass Spectrometer