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    DIAGNOSTIC TESTING
    Microbiology
    Culture, ID and susceptibility workflows
    Spatial & Multi-Omics
    Emerging assays with complex genealogy
    Flow Cytometry
    Panel-based phenotyping with gated review
    Immunoassays
    ELISA and plate-based testing at scale
    Proteomics
    MS-based protein workflows with instrument capture
    Histopathology
    Block, slide and stain tracking end to end
    Cytogenetics
    Karyotype, FISH and CMA case management
    Molecular Diagnostics
    PCR and molecular assays, validated flows
    NGS
    Sequencing workflows from library prep to sign-out
    ANALYTICAL QC
    Batch Execution & Release
    EBR, release and CoA generation
    Raw Materials
    Receipt, CoA and disposition
    Bioassay & Potency
    Cell-based and binding potency assays
    Stability Studies
    Protocol through pull point to trend
    Environmental Monitoring
    Scheduling, trending and alerting
    Microbiological QC
    Sterility, endotoxin and bioburden
    Physical Testing
    Hardness, particle size and integrity
    Wet Chemistry
    Titration, water content and bench chem
    Spectroscopy
    ID testing and compendial spectroscopy
    Mass Spectrometry
    Trace impurities and characterization
    Dissolution
    Performance testing with staged criteria
    Chromatography
    HPLC and GC testing against spec
    GMP BIOMANUFACTURING
    Batch Execution & Review
    Review by exception, not by binder
    Fill-Finish & Packaging
    Aseptic filling through serialization
    Weigh & Dispense
    Check-weigh dispensing with genealogy
    Buffer & Media Prep
    Recipe-driven prep with expiry control
    Downstream Processing
    Capture, polish and viral clearance
    Upstream Processing
    Seed train to harvest with online data
    mRNA & Nucleic Acid
    IVT through LNP formulation
    Viral Vector Production
    AAV and LV from transfection to titer
    Cell Therapy Manufacturing
    Vein-to-vein COI and batch execution
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