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Designed for GxP Precision, Compliance, and Confidence

Confident data. Defensible workflows. Audit‑ready systems.

As pharmaceutical programs move from discovery into regulated development, data must do more than inform science—it must withstand regulatory scrutiny. The SpectraMax® i3x platform, powered by SoftMax® Pro GxP Software and supported by validation services, is engineered to support reproducible, traceable data generation within controlled workflows. This helps teams carry data forward with confidence as development complexity and compliance expectations increase.

Why regulated pharmaceutical labs choose SpectraMax® i3x?

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Data integrity by design 

Engineered to support reproducible, traceable, and defensible data in GxP‑regulated pharmaceutical environments—where data integrity is non‑negotiable.
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Performance That Scales 

Sensitive, multi‑mode detection with a modular architecture that supports evolving assay requirements while maintaining controlled, validated workflows.
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Confident, audit-ready results

Consistent workflows and reproducible performance help teams generate data they can trust—and confidently defend during audits and inspections.
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Validation and Support

SoftMax® Pro GxP Software, validation documentation, and expert support services help pharmaceutical labs meet ongoing compliance and data integrity requirements.

Talk to a GxP Compliance Specialist

Tell us about your lab and compliance needs and a Molecular Devices specialist will follow up with information tailored for regulated environments.

 

We support GMP, GLP, and other regulated laboratory settings worldwide.


 

Start consultation. Claim your discount.

No obligation. Speak with a specialist familiar with regulated pharma workflows.

Real Scientists. Real Impact.

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Molecular Devices: A life science company

We journey alongside researchers, combining next-gen technology and deep expertise to spark bold breakthroughs that push research boundaries and transform lives worldwide.

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