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Your analysis is only as reliable as the sample

Laboratories can measure with extreme precision, but no analytical method can correct for an unrepresentative sample. Yet the results often receive more attention than the way the sample was collected. This is a significant risk: a well-written report can give a false sense of security if the sampling does not adequately reflect the batch, the process, or the hazard being investigated.

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An employee inspects fresh tomatoes in a crate during a quality control check. The image illustrates food safety, product quality, and inspections of fresh produce.

Representativeness starts with the research question

A good sampling plan doesn’t start with the number of samples, but with the decision you want to make based on the results. Do you want to release a batch, monitor a process, evaluate a supplier, or identify a potential source of contamination? Each question requires a different approach. A sample suitable for trend monitoring is not automatically sufficient to make a confident decision about an entire batch.

Therefore, first map out the batch composition and the potential distribution of the hazard. Is the contamination homogeneous, or could it occur locally? Are there differences between the beginning and end of a run, between pallets, package sizes, or production zones? Microbiological hazards and allergens, in particular, can be unevenly distributed. In such cases, a single small sample could easily be taken from a location other than the relevant one.

A lab technician wearing protective gloves cuts a red bell pepper for analysis in a laboratory setting. The image illustrates food safety, quality control, and the testing of fresh produce.

More samples aren't always better

A larger number of samples only increases certainty when locations, times, and quantities are selected in a targeted manner. Random additional sampling without taking process variation into account can repeat the same blind spot. The added value lies in a plan that accounts for the heterogeneity of the batch and deliberately includes the moments of highest risk.

Document how primary samples are selected, whether they are analyzed individually or as a composite sample, and what implications this has for detection and interpretation. A composite sample can be efficient for an average composition but may dilute a local deviation. Individual samples provide more information about variation but require more analyses and a pre-agreed decision rule.

Control the steps prior to analysis

The reliability of a sample can be compromised as early as during collection, packaging, transport, or storage. Non-sterile equipment, insufficient homogenization, a broken cold chain, or excessively long turnaround times can affect the results. Identification errors and incomplete documentation also make it difficult to justify the results.

Therefore, treat sampling as a critical process. Work with clear instructions, appropriate materials, and trained staff. Record who took the sample, where and when it was taken, which batch it came from, and under what conditions it was shipped. Include relevant deviations so that the laboratory and QA can evaluate the results in the proper context.

Use uncertainty as input for your decision

An analysis result is not an absolute judgment about every product in a batch. It is information derived from a limited portion of that batch, obtained using a method that itself is subject to variation. Therefore, combine the results with process knowledge, supplier history, previous results, complaints, and other verification data. The greater the potential impact of a false-negative conclusion, the stronger the justification for the sampling plan must be.

Furthermore, a robust plan is evaluated regularly. When processes, volumes, suppliers, or risks change, the sampling plan must adapt accordingly. By critically assessing not only the analysis but also its representativeness, QA ensures that a laboratory result serves as a solid foundation for decision-making.

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