How to select samples for testing and not redo the test report
A sample is not "any unit from the warehouse". Whether the test report is suitable for the document depends on how the sample was selected and recorded.
AGAI Galochka editorial team05 min
Formally, sample selection is a half-hour procedure. In practice, this is where weeks are lost, when it turns out that the test report does not fit the required scheme.
What sets the rules for sample selection
Three factors
01SchemeA series or a batch, and who selects
02Testing programHow many units and in what condition
03Typical representativeWhich modification represents the product line
The typical representative is chosen by the worst case: if it passes the tests, the other modifications are considered confirmed.
What is recorded in the sampling record
Name of the product and the designation of the modification
Date and place of sampling, and which batch it is from
Number of units selected
Who selected them and in whose presence
Conditions of transport to the laboratory
About packaging
Samples are handed to the laboratory in their retail packaging and complete set, including the instruction: some requirements of the regulation apply specifically to the packaging and the operating documents.
Typical mistakes
How time is lost
Sending a single unit — it is not enough for destructive tests
Taking a sample from a pilot batch for a serial-production scheme
Sending the product without packaging and instruction
Not drawing up a sampling record
How to do it right
Confirm the number of units in advance, according to the testing program
Select from serial products made by the approved technology
Assemble the set the way the product will reach the buyer
The evidential value of the test report depends on this, and the difference is visible in any dispute.
Who selects
When it is used
Weight
Representative of the testing laboratory
Schemes with sampling at the site or on the market
Highest: the sampling is recorded by an independent party
Representative of the certification body
Certification of serial products
High
The applicant on their own
Some declaration schemes
Sufficient, but the responsibility lies fully with the applicant
Selecting the samples yourself is cheaper and faster, but during a check this is exactly where questions arise: what proves that the product tested is the same one you produce. The answer is given by the sampling record and careful identification of the sample.
The sample must come from the series, not be made "for testing"
Making a specially neat unit is an understandable temptation and a direct path to an invalid test report. What is tested is what is actually produced: with the same raw materials, on the same equipment, in the same shift.
How many samples are needed
The exact number is set by the laboratory based on the test methods, but the logic is always the same, and it is useful to understand it in advance — so as not to send one unit where six are needed.
Destructive tests. The sample is consumed: strength, flammability, chemical analysis. A reserve is needed.
Several groups of indicators. Microbiology, physical chemistry and toxicology are often done in different departments and need their own units.
Arbitration sample. Part of the samples is kept in case of a dispute — this is normal practice.
Different modifications. If the document covers several models, the typical representative is tested, and sometimes each model.
Packaging. For products where contact with the packaging matters, the sample is supplied in consumer packaging, not loose.
Confirm the number before sending: sending more samples later extends the timeline more than it seems, especially if the product comes from abroad.
How to deliver the sample without losses
Testing starts with acceptance, and some samples are rejected at this stage.
The packaging protects against damage: a broken sample cannot be tested
For products with a temperature regime — keep the cold chain, otherwise microbiology will show the wrong result
The marking on the sample is intact and readable: it is used to identify the sample
Information on the batch, the date of manufacture and the expiry date is attached
The sample is not opened, if the method requires intact packaging
For imports — the samples were brought in legally, with proof of origin
What to record for the future
A year later, when an inspection control or a dispute with a buyer arrives, it is impossible to remember the details of the sampling. So right after the sampling it is worth saving:
The sampling record with the date, place, batch number and signatures
Photographs of the sample and its marking
Information on which batch and shift the sample was taken from
Who selected it and on what basis
Where it was sent and what remained in storage
This set should be kept next to the test report: together they answer the main question of the inspector — whether the test relates to the product that lies on the shelf. How to check the laboratory itself and its accreditation scope — in a separate article.
Check your product
Describe your product in plain words — the system will show the expected HS code (TN VED), the applicable regulations and the set of documents. Start the check.
This material is for information only and does not replace advice from an accredited certification body.