Industry
Biotech & Pharma — software-defined liquid handling
Software-defined liquid handling for biotech & pharma R&D.
Your challenges
What this industry needs from liquid handling.
Cell culture, perfusion and bioprocess development demand reproducibility, parallelism and clean, audit-ready data — exactly what a software-defined system delivers.
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Reproducibility across runs
Manual feeds, sampling and pH/DO adjustments drift between operators and shifts, making results hard to reproduce and compare.
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Parallel experiments
Running many conditions at once multiplies hands-on load and the risk of a missed or mislabeled intervention.
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Audit-ready data
R&D heading toward GMP needs traceability, e-signatures and access control — not spreadsheets and device-local logs.
Processes
Where QB fits your work.
Start from your process — each one maps to the system classes that run it.
What changes with QB
What good looks like.
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Reproducible by design
Feeds, sampling and control loops run from versioned recipes, so every run executes the same way.
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More conditions, same team
Parallel processes are orchestrated from one platform, so headcount doesn't cap throughput.
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Compliance-ready
Audit trail, e-signatures and role-based access (21 CFR Part 11 / ISA-18.2) travel with the data.
Scale
Works at every scale — screening to pilot, and beyond with partners.
More industries
Explore other industries.
Bring software-defined liquid handling to Biotech & Pharma.
Schedule a demo. See how to accelerate and automate your bioprocesses.
Contact us
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