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Validation Services

Validation Support Built for Real Laboratory Launches

SMG helps laboratories plan, document, and execute validation work with practical support that keeps the focus on go-live readiness and audit confidence.

Limit of Detection Studies

Determine analytical sensitivity with support for practical validation planning.

Accuracy Studies

Confirm clinical performance against expected targets and comparator workflows.

Precision Studies

Assess repeatability and reproducibility across operators, runs, and instruments.

Stability Studies

Validate reagent, specimen, and run stability within your operating environment.

Cross-Reactivity

Reduce false positives by reviewing organism and target interaction risk.

Interference Studies

Evaluate matrix and specimen interference before routine launch.

Method Correlation

Compare performance with your current molecular or culture workflow.

Instrument Verification

Confirm instrument readiness and setup before go-live.

SOP Development

Build practical SOP language for bench-ready implementation.

Staff Training

Train operators on assay setup, workflow discipline, and troubleshooting.

Inspection Readiness

Prepare documentation and processes for CLIA/CAP-ready environments.

Validation Reports

Deliver clear documentation to support sign-off and internal review.

On-Site Support

Work alongside laboratory teams during launch and early operation.

Implementation Support

Validation and launch support that feels organized from day one

Whether your lab needs a narrow assay verification plan or a full implementation package, SMG can help build the path from validation planning to inspection readiness.