What We Do
Services Built for the Analytical Lab
From analyst training and method development to QA/QC programs and regulatory compliance — LabWorx delivers bench-level expertise across the full laboratory lifecycle.
Technical Consulting
We develop your analysts and your processes. Hands-on training, method development, workflow optimization, and continuous improvement — the technical foundation your laboratory needs to perform at the highest level.
Quality & Compliance
Quality is built into everything we do. QA/QC programs, CAPA, data integrity, method validation, and regulatory compliance support — keeping your lab audit-ready and your data defensible.
Technical Consulting
Building Better Labs from the Bench Up
Analyst Training & Development
Our flagship service. We develop chemical analysts from the ground up — building competency in instrumentation, technique, data interpretation, and best practices.
- Hands-on training with GC, LC, IC, ICP, spectroscopy, titration, and more
- Instrument-specific operation, maintenance, and troubleshooting
- Sample preparation techniques and best practices
- Data analysis, interpretation, and reporting
- Competency assessments and documentation
- Onboarding programs for new analysts
- Continuing education for experienced staff
Analytical Method Development
Design and develop robust, fit-for-purpose analytical methods tailored to your matrix, regulatory requirements, and instrumentation.
- Method design from concept through optimization
- Matrix-specific method development (environmental, food, pharma, industrial)
- EPA, FDA, ISO, and NELAC method adaptation
- Method transfer between instruments or laboratories
- Selectivity, sensitivity, and robustness optimization
- Documentation and SOP development
Laboratory Workflow Optimization
End-to-end workflow consulting across the full analytical process — eliminating bottlenecks, reducing error, and improving throughput.
- Sample receipt, login, and chain-of-custody review
- Sample preparation workflow design and optimization
- Instrumentation sequencing and batch scheduling
- Data review and reporting workflow streamlining
- Risk identification and mitigation strategies
- Turnaround time improvement
- Cross-training and backup coverage planning
Continuous Improvement (CIP)
Identify inefficiencies and implement sustainable improvements across your analytical operations using proven best practices.
- Laboratory performance gap analysis
- Root cause analysis for recurring issues
- Process redesign and standardization
- Best practice benchmarking across industries
- Staff engagement and change management support
- Metrics development and KPI tracking
Quality & Compliance
Defensible Data. Audit-Ready Programs.
QA/QC Program Development & Support
Build or strengthen your quality assurance and quality control programs to meet regulatory expectations and produce defensible data.
- QA/QC program design and implementation
- Control chart development and statistical monitoring
- Blank, spike, duplicate, and standard review protocols
- Laboratory control sample (LCS) program development
- Proficiency testing support and corrective action
- Internal audit preparation and support
Compliance & Regulatory Support
Navigate EPA, FDA, ISO 17025, NELAC/TNI, and state/local requirements with confidence — from initial setup through inspection readiness.
- EPA method compliance (SW-846, 500-series, 600-series, 8000-series)
- FDA 21 CFR Part 11 and cGMP analytical support
- ISO 17025 and NELAC/TNI accreditation preparation
- State and local regulatory requirement interpretation
- Regulatory gap assessments
- Inspection readiness reviews
- Response to regulatory findings and observations
CAPA Development & Implementation
Structured corrective and preventive action programs that address root causes — not just symptoms — and prevent recurrence.
- Root cause analysis (RCA) facilitation
- CAPA plan development and documentation
- Effectiveness check design and monitoring
- Out-of-specification (OOS) investigation support
- Deviation and non-conformance management
- Trend analysis and proactive CAPA identification
Method Validation & Review
Comprehensive method validation, verification, and review services to ensure your methods are fit for purpose and regulatory compliant.
- Full method validation (accuracy, precision, linearity, LOD/LOQ, selectivity, robustness)
- Method verification for adopted reference methods
- Comprehensive data and method review
- Method SOP development and revision
- Single-laboratory validation studies
- Validation report preparation
Data Integrity Programs
Establish and maintain data integrity frameworks that meet regulatory expectations and protect the defensibility of your analytical results.
- Data integrity gap assessment
- ALCOA+ principles implementation
- Electronic and paper record review procedures
- Audit trail review protocols
- Data integrity training for laboratory staff
- Remediation support following data integrity findings
Regulatory Frameworks & Standards We Work With
Common Questions
Frequently Asked
Ready to strengthen your lab?
Whether you need a training program, a method developed, or a compliance program built from scratch — let's talk about what your lab needs.