Industries We Serve: Automated Compliance for Life Sciences

Validator empowers pharmaceutical, biotech, medical device, nutraceutical, and FDA/GxP regulated organizations with audit-ready compliance and digital validation tailored to every industry’s needs.

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Built for Complex Regulatory Challenges. Chosen by Life Sciences Leaders.

Validator helps regulated organizations of every size achieve audit-ready compliance, streamline validation, and confidently manage change—even as regulations, products, and pressures evolve. Our automation platform flexes to fit your industry’s requirements and supports every validation team striving for quality, efficiency, and measurable business improvement.

Why Industries Choose Validator

Unlike other platforms, Validator is built, implemented, and supported directly by the professionals who designed it. That means you always work with the experts—no partner handoffs, no support surprises, and no vendors who “just sell” but don’t deliver.Validator isn’t just documentation digitized—it’s true process automation, end-to-end.

What sets Validator apart:

Direct Implementation: Validator is the only platform built and implemented by its own creators. No partners, no confusion, and a support team that knows your industry challenges first-hand.

True Automation, Not Just Digitization: Competitors move paper to a screen. Validator fully automates protocols, approvals, risk assessment, traceability, and change control—reducing your manual work and audit anxiety.

100% Client Referenceability: Every Validator implementation is a success story, and every client is willing to share their results and experience.

Regulatory Alignment: Validator is purpose-built for FDA, EMA, and GxP compliance, with built-in CSA-first workflows and rapid response to changing global guidelines.

Transparent Pricing: SaaS or enterprise license, with every feature for every client—no minimums, no upcharges, and no hidden fees.

Seamless Integration: Validator connects easily to your LIMS, MES, ERP, and core business systems, so your data and compliance efforts are always unified.

Unmatched Accountability: With Validator, there is always one team responsible—the team that built it.

Industries We Serve

Validator is trusted by leaders across all life sciences sectors. Our industry-specific solutions ensure that—whatever your field—compliance doesn’t get in the way of progress:

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Pharmaceuticals

Keep new molecules moving from lab to market with audit-ready CSV, process, and equipment validation. Validator is built for high-volume complex pharma operations—cutting cycle time, reducing errors, and keeping every record accessible for inspection.

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Biotechnology

From gene therapy to vaccines and next-gen biologics, Validator adapts to the fastest-moving teams. Automate validation for evolving products, support rapid scale-up, and make compliance seamless—even with small teams and short timelines.

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Medical Devices

Rely on Validator for full equipment qualification, design history documentation, and QMS compliance. Simplify multi-site global operations, meet ISO and FDA demands, and connect device teams to unified validation data.

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Life Sciences

Validator streamlines compliance for nutraceutical and supplement manufacturers—automating validation, supporting GMP and FDA requirements, and keeping every record audit-ready as your product portfolio grows.

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FDA/GxP Regulated Organizations

Validator is the smart choice for diagnostics, CROs, specialty manufacturing, and any setting that requires traceable, inspection-ready validation. Streamline legacy migrations, manage multiple regulations, and ensure complete oversight—no matter how complex your business.

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What You Can Automate with Validator

All modules are fully configurable and integrate directly with your LIMS, MES, ERP, and other business systems—no custom development needed.

Computer System Validation (CSV)

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Manage approvals and execution with real-time updates. Automatically generate protocols, risk assessments, and traceability matrices. All compliant with Part 11 and GxP.

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Process Validation (PV)

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Map, track, and automate all three stages of process validation (design, qualification, verification). Manage batch records and trend data with integrated reporting.

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Equipment Qualification (EQ)

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Never scramble for documents again with IQ, OQ, PQ oversight, calibration, and change control in one place.

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Cleaning Validation

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Standardize and automate cleaning procedures, scheduling, and documentation to stay ready for any inspection.

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Compliance That’s Proactive, Integrated, And Ready For What’s Next

Not all platforms are created equal. Validator is shaped by experience—built and implemented by people who have worked inside life sciences teams, led audits, and solved real regulatory problems. 

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Constant Compliance


Real-time dashboards create a living audit trail, so your team works from current data and your compliance stays inspection-ready. 

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Integrated With Your Systems


Every connection is fully configurable to your LIMS, ERP, MES, HR, finance, and risk systems with no custom code, so you can access and personalize without calling IT.

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Fast ROI with Proven Efficiency


Achieve over 40% efficiency gains and 100% implementation success. Fast ROI with Validator fully configured and running smoothly within 3 months.

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Always Up-to-date


As regulatory standards evolve, so does Validator, to ensure your validation system follows CSA and globally aligned practices for international compliance.

Testimonials

Here are a few of our client and their testimonials

Validator takes a systematic approach to the process of validation. With no ambiguities in the process audits are easy to defend and information is easily accessible.
Han Duong
Director of Information Systems
We had the added benefit of working alongside the creators of the software. The product was so responsive to our needs that it was like having a custom tool built to fit the matrix of our business.
Alexia Pico
Supervisor, Development Translational Medicine
Validator helps someone without a complete knowledge of computer system validation get up to speed and become a contributing team member faster, because they have all the tools and templates available, and know where to find everything they need.
Steris

Instead of physical documents being moved throughout our organization globally, being printed and rescanned six or more times, compliance document reviews and approvals will now take only minutes. Compliance and integrity is improved, because we are able to keep documents and information uncorrupted by human error.

Sachin Bhandari
Global Head Compliance at SunPharma
We understood that implementing better technology would help us perform validation with greater ease, speed and efficiency.
Esra Guven
Principal Consultant for the Systems Qualification & Compliance Group
Validator is helping us complete validation projects better than before.
Alok Varshney
Manager of the Systems Qualification & Compliance Group