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Engineered for data integrity in GxP-ready CRO labs

Generate high‑quality, reproducible data with a flexible microplate reader platform designed to support data integrity, traceability, and evolving compliance needs as biotech programs advance.

For GxP‑ready contract research organizations, credibility is built on the ability to generate data that sponsors and regulators can rely on across studies, programs, and inspections. The SpectraMax® i3x multi‑mode microplate reader—powered by SoftMax® Pro GxP Software and supported by validation documentation and expert services—is engineered to help CRO labs produce reproducible, traceable, and defensible data within controlled workflows. By supporting consistency and transparency as regulatory expectations increase, the SpectraMax i3x platform helps CROs maintain confidence in their data—and in the services they deliver.

Why CROs choose the SpectraMax® i3x reader for regulated workflows

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Data integrity by design

Engineered to support reproducible, traceable, and defensible data across GxP‑regulated CRO workflows—where data must stand up to sponsor audits and regulatory inspection.
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Performance that scales

Sensitive, multi‑mode detection with a modular platform that supports diverse assay types while maintaining standardized, controlled workflows across multiple studies and sponsors.
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Confident results

Reproducible workflows and reliable performance help CROs generate data sponsors can trust—and confidently include in regulatory submissions.
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Validation and Support

SoftMax® Pro GxP Software, validation documentation, and expert support services help CROs maintain inspection readiness and meet ongoing compliance expectations across clients and studies.

Plan your path to inspection‑ready GxP workflows

Tell us about your assay types, study mix, and regulatory requirements. Our specialists will help you evaluate a SpectraMax® i3x reader workflow designed to support data integrity, consistency, and audit readiness across CRO programs.



Supporting sponsor audits, regulatory inspections, and multi‑study environments.

Start a CRO focused GxP-focused consultation

No obligation. Conversations tailored to biotech programs at different stages of development.

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