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Dry Labbing

Testing

Also known as: Dry Lab, Fabricated Results, COA Fabrication, Test Result Falsification

Fabricating or falsifying laboratory test results without performing the actual analysis.

What It Means

Dry labbing is the practice of issuing test results — typically in the form of a Certificate of Analysis — without actually performing the analytical work, or falsifying results to produce a desired outcome. In the supplement industry, dry labbing has been documented in FDA warning letters and enforcement actions. The June 2024 FDA warning letter to West Coast Laboratories cited failures to conduct required identity testing and verify test results, demonstrating how the practice manifests in real regulatory action. Dry labbing undermines the entire testing infrastructure: a brand using a dry-labbed COA to demonstrate compliance is unknowingly building on fabricated evidence. The practice is particularly insidious because the output (a professional-looking COA) is indistinguishable from legitimate results without independent verification.

What It Is Not

Dry labbing is not carelessness, analytical error, or method variability. It is intentional fraud. It is also not limited to small or disreputable labs — the incentive structure exists wherever labs face price pressure, volume demands, or client relationships that discourage unfavorable results. ConsumerLab has documented cases where manufacturers pressured testing labs to refuse work with independent evaluators, illustrating the commercial dynamics that enable the practice.

Evidence and References

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