Knowledge / General guidance

Technical context for better questions.

Understanding ISO/IEC 17025

What manufacturers should know about laboratory competence, traceability and reliable reports.

Why it matters

ISO/IEC 17025 addresses competence, impartiality and consistent laboratory operation. For a client, the important question is not simply whether a standard is named, but whether the relevant matrix, method and decision are properly defined.

Before commissioning work

Confirm the product matrix, target market, applicable specification, required evidence and intended use of the report. Clear context supports appropriate method selection and more useful reporting.

Food allergen testing explained

A practical view of allergen risk, sampling, methods and supplier control.

Testing is one part of control

Useful allergen evidence begins with ingredients, supplier information, shared equipment, cleaning controls and the specific allergen of concern. Sampling must reflect where contamination could occur.

Define the decision

State whether testing supports investigation, verification, supplier control or a label decision. Product-specific requirements and interpretation limits should be confirmed during technical review.

Shelf-life study essentials

Designing studies around storage, packaging and expected product use.

Model the real product journey

A study should reflect expected storage conditions, packaging, distribution, opening and consumer use. Relevant microbiological, chemical and sensory questions depend on the product and its risks.

Plan before sampling

Define time points, conditions, acceptance criteria and report purpose before the study begins. Alpha Chemicom can help translate these assumptions into a practical evidence plan.

General guidance is a start.
Your matrix defines the detail.

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