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Quality Control Resources

Everyday QC, simplified

Ease QC complexity, simplify daily workflows, and improve laboratory performance.

Simplify QC workflows

  • Reduce workflow complexity and manual burden
  • Simplify daily QC operations

Accelerate decisions

  • Identify priority issues faster
  • Focus where it matters most

Sustain QC performance

  • Benchmark performance
  • Drive continuous improvement and standardization

Featured

Results are in for the 2026 Global QC Survey! Review key findings and best practice recommendations for optimizing QC workflows.

Cut your QC—not your confidence. This practical SmartNote explains how laboratories can use their own performance data and Westgard Sigma Rules to reduce false rejections, streamline troubleshooting, and make QC more efficient.

On-demand demo! Experience an expert walkthrough of LabLink 360 quality assurance software.

Continuous quality improvement

It’s not me, it’s MU! Measurement uncertainty in the US and around the world.

In this webinar, industry expert Sten Westgard, MS, of Westgard QC, Inc., provides key findings, challenges, and takeaways about QC practices across the globe. Presented at ADLM, 2024.

Practical strategies for optimizing QC workflows and recommendations for best practices.

Written by expert Sten Westgard, MS, of Westgard QC, this quality control implementation guide builds on the findings from the 2025 Global QC survey to provide real-world strategies for modern laboratories.

Improve your QC practices

Smart Note | Peer Group Comparison

Written by expert Sten Westgard, MS, of Westgard QC, this SmartNote explains why peer group quality matters more than peer group size and how laboratories can use meaningful comparisons to improve QC performance.

SmartNote | Sten Westgard

A warning on warning rules: Are we warning ourselves to distraction?

The background and limitations of 2 standard deviation (2SD) "warning rules" and the advantages of Westgard rules.

Guide | Sten Westgard

Smarter QC for stronger labs: A practical guide to modern quality control

A stepwise implementation guide for optimizing QC workflows and practices.

SmartNote | Sten Westgard | US Edition

The state of laboratory QC in 2025: Challenges and opportunities

Results from the Westgard 2025 global QC practices survey, presented with key

findings, regional trends, and best practice recommendations for optimizing QC.

SmartNote | Sten Westgard | European Edition

The state of laboratory QC in 2025: Challenges and opportunities

Build your QC knowledge

SmartNote

How consolidation of QC references improve clinical laboratories’ operational efficiency

Explore a real case scenario and discover how Thermo Scientific™ MAS™ quality controls can help laboratories improve their day-to-day QC efficiency.

SmartNote | MAS Quality Controls Consolidation

This SmartNote presents a laboratory case study on consolidating quality control references with Thermo Scientific MAS products. It describes potential efficiency gains, including fewer daily QC bottles and lot-to-lot validations, and simpler purchasing, storage, and QC management. Results may vary by laboratory workflow and configuration.

SmartNote | MAS Quality Controls Workflow

This SmartNote offers a five-stage framework for examining daily QC workflows, from preparation and testing through review, release, and ongoing monitoring. It helps laboratories identify where time, materials, repeats, and complexity accumulate, and consider how method performance can inform QC rules and practices.

Thermo Scientific MAS Max Handling

Thermo Scientific™ MAS™ Max controls stored at -15 to -25°C

Software Flyer | Thermo Scientific LabLink 360

This flyer introduces Thermo Scientific LabLink 360 quality assurance software, showing how centralized QC insights, customizable alerts, and cross-site comparisons can help laboratories review results more efficiently, focus on priority issues, and make confident decisions.

Discover how qualified laboratories can participate in the Thermo Scientific™ MAS™ QC Value Assignment Program.
Review testing guidelines, participation requirements, timelines, and available compensation options.

Not all products are CE marked or have FDA clearance for sale in the U.S. Availability of products in each country depends on local regulatory marketing authorization status.