Life Sciences Compliance Automation
Validator streamlines validation, centralizes documentation, and keeps your operations audit-ready—empowering life sciences teams across diagnostics, research, and specialty manufacturing.
Compliance Automation for Every Life Sciences Environment
Life sciences organizations are at the forefront of advancing health, innovating diagnostics, and launching transformative therapies. Whether you’re running a contract research organization, specialty pharmaceutical, diagnostics lab, or a clinical trial operation, compliance lives at the heart of your business. But diverse requirements, multi-system environments, and evolving regulations make it challenging to keep validation and documentation streamlined, error-free, and audit-ready.
Validator gives all life sciences teams—from research through manufacturing—a single platform to automate critical validation tasks, manage documentation, and ensure ongoing compliance no matter how complex your workflows or fast your field moves. Designed by experts and proven across the industry, Validator helps reduce manual workload, prevent findings, and support your mission to improve patient outcomes.
A Fit for Every Life Sciences Workflow
Validator is built to solve the specific challenges of high-mix, multi-site, and innovation-driven life sciences companies:
- Automated Validation Across All Operations: Manage equipment, process, cleaning, and system validation with automated protocols, records, and approvals—customized to your company’s needs.
- End-to-End Data Management: Centralize validation documentation, manage legacy system decommissioning, support seamless digital record conversion, and maintain a unified audit trail.
- Seamless System Integration: Validator connects across ERP, LIMS, content/data management, and lab automation—ensuring every compliance document and record is always up to date, accessible, and ready for inspection.
- Scalable for Growth:
Modular design means you can add validation areas or expand to new sites and teams without overwhelming your compliance operations or staff.
Technical Standards You Can Count On
- Complete GAMP 5 V-Model, CSA-first, 21 CFR Part 11, and EU Annex 11 compliance
- Role-based permissions and e-signature for document control
- Built-in change control workflows and audit trails across every site and system
Business Impact for Life Sciences Leaders
- Reduce Error and Risk: Centralize and automate compliance so you’re ready for audits—no more lost records or last-minute scrambles.
- Save Time and Resources: Teams see up to 40% efficiency gains and reduced documentation burden across the entire business.
- Flexible for Every Project: From high-volume diagnostics to specialty product launches, Validator adapts to unique client workflows.
- Client-Proven Trust: Life sciences organizations across diagnostics, research, and specialty pharma rely on Validator for audit-ready compliance, measurable efficiency gains, and consistent, referenceable success stories.
Who Benefits?
Diagnostics labs, CROs, specialty manufacturers, and all fast-moving, highly regulated life sciences organizations.
Tailored Automation For Every Validation
Validator is designed to tackle your biggest compliance pain points either one process at a time or across your entire validation lifecycle.
Explore each core solution to see how Validator can streamline your work and strengthen your audit confidence.
Computer System Validation (CSV)
Validator automates every phase of system validation, from protocol creation to risk management and compliance documentation. Records and traceability are built in and reliable, keeping your systems audit-ready at all times.
Process Validation (PV)
Experience more control and fewer surprises with automatic protocols, batch records, and trend data integration. All three stages of process validation—design, qualification, ongoing review—move faster and smarter with Validator.
Equipment Qualification (EQ)
Keep every asset documented and up to date. From installation through annual verification, Validator manages every protocol, document, and calibration so you’re always ready for inspection.
Cleaning Validation
Cleaning schedules, procedures, and proof are managed for you. Auditors get instant access to every record, while your team has more time for high-value work.
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.
Constant Compliance
Real-time dashboards create a living audit trail, so your team works from current data and your compliance stays inspection-ready.
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.
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.
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.
Frequently Asked Questions
Can Validator support compliance for a variety of life sciences organizations, including CROs, diagnostic labs, and specialty manufacturers?
Yes. Validator is flexible and configurable to support diverse life sciences environments, including contract research organizations (CROs), diagnostics labs, and specialty pharma manufacturers—ensuring tailored compliance and validation across different workflows.
How does Validator help manage and centralize documentation from multiple sites and systems?
Validator centralizes all validation documents, records, and audit trails in one secure platform—making it easy to access, organize, and retrieve records for audits, no matter how distributed your teams or facilities.
Is Validator capable of migrating legacy data and supporting digital records conversion?
Absolutely. Validator supports smooth archiving, legacy system decommissioning, and conversion to digital records, helping organizations modernize and maintain data integrity during transitions.
What benefits can life sciences teams expect in terms of efficiency and compliance improvement?
Life sciences teams using Validator typically experience significant reductions in manual workload and documentation errors, improved audit outcomes, and faster, more reliable compliance processes—freeing staff to focus on research and innovation.
Testimonials
Here are a few of our client and their testimonials
