Standards & accreditation

ISO/IEC 17025 test item handling: sample identification and chain of custody

If a test item cannot be identified unambiguously or nobody knows who held it last, every result is open to challenge. This guide shows what clause 7.4 requires and how to document receipt, identification and handovers without gaps.

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In short

ISO/IEC 17025:2017 requires in clause 7.4 that the laboratory has a procedure for transport, receipt, handling, protection, storage, retention and disposal or return of test items. Every item is uniquely identified, and the identification is retained throughout the laboratory's possession. On receipt, deviations from the described condition are recorded; if there is doubt about suitability, the laboratory consults the customer before starting. Where environmental conditions affect validity, they are maintained and recorded. In practice this means: a unique ID on the item, a documented condition on receipt, and a gapless chain of holder, location and time.

What a test item is and why 7.4 draws attention

A test item is anything the lab tests, calibrates or samples: a component, a battery cell, a specimen, a device or a sample. The standard does not distinguish by size or value. Clause 7.4 ensures that a result really belongs to the item the customer sent, and that it was not altered in transit or in the lab.

Assessors like to check this by example: they take a test report, follow the ID back to receipt and ask where the item was and who held it in between. Gaps show quickly because they cannot be closed retroactively.

What clause 7.4 requires

  • Procedure: A documented approach for transport, receipt, handling, protection, storage, retention and disposal or return.
  • Unique identification: Every item is clearly marked; the ID is retained for as long as the item is in the lab, including sub-samples.
  • Traceability: The identification prevents confusion with other items, physically and in the records.
  • Abnormalities on receipt: Deviations from the described condition or from the test specification are recorded.
  • Consultation: If there is doubt about suitability, the customer is consulted before testing starts, and the conversation is documented.
  • Environmental conditions: Where storage or handling must meet specific conditions, they are maintained and recorded.

Minimum records at receipt

Receipt is the moment the chain begins. What is missing here cannot be collected later. Every receipt should contain:

RecordWhy it is needed
Unique IDLinks item, measurement data and report; rules out mix-ups
Customer type and serial numberMatches the item to the order and the test report
Time and receiving personStart of the chain of custody
Condition on receiptDamage, missing parts, deviations from the description
PhotosObjective evidence of the incoming condition
Storage location and conditionsProof that required conditions were maintained
Order or projectAssignment to the test order
Planned return or disposalSettles what happens to the item at the end

Building the chain of custody in six steps

  1. 1

    Define the ID scheme

    A scheme that stays unique, for example year plus running number, plus a code you can print as a barcode or QR label. Customer serial numbers are additional data, not the ID.

  2. 2

    Label the item at receipt

    Immediately on arrival. If the item itself cannot be labelled, mark the packaging and document that.

  3. 3

    Record the incoming condition

    Capture condition, abnormalities and photos in the same step, not later from memory.

  4. 4

    Record every change

    Handover to a colleague, relocation, shipment to an external lab: every change of holder or location is an event with time, person and place.

  5. 5

    Check the status before testing starts

    The tester scans the item, sees holder, location and incoming condition, and confirms it matches the order.

  6. 6

    Close the chain properly

    Record return or disposal as the final event, with date and responsible person; only then is the chain closed.

Typical audit findings

  • An item carries no ID, or the ID is only on the packaging, which was thrown away.
  • The incoming condition is not documented; damage cannot be attributed to transport or to the lab.
  • Testing started despite doubts about suitability, without documented consultation with the customer.
  • Location and holder are not evidenced for the periods between two test steps.
  • Required storage conditions (temperature, state of charge, humidity) were not recorded.
  • Return or disposal cannot be traced; the chain ends without closure.

Tools: spreadsheet, label or item management

A spreadsheet is enough as long as everyone maintains it, every entry carries date and person, and nothing is overwritten. In practice discipline is what fails: entries are added later, changes can no longer be traced. An item management system takes that burden off you if it offers three things:

  • Mandatory holder and location on every event, so no gaps arise.
  • A scannable code that leads directly to the item's detail page.
  • A change history that keeps deleted or corrected entries traceable.

TestLabIQ keeps a chain of custody per test item with events (received, handed over, relocated, returned, disposed), mandatory holder and location fields, photos per event and a scannable short code for barcode or QR labels. Backdating and deletions remain visible in the audit log. Measurements can be linked directly to the item's page. TestLabIQ does not capture environmental conditions during storage automatically; record climate data as a note on the event or keep it in your climate monitoring system.

Frequently asked questions

What does ISO 17025 clause 7.4 require?

A procedure for transport, receipt, handling, protection, storage, retention and return or disposal of test items, unique identification throughout, recording of abnormalities on receipt, and consultation with the customer when suitability is in doubt.

What does sample identification under ISO 17025 involve?

A unique ID that cannot be confused with other items, attached to the item or its packaging and retained until the order ends, including the assignment of sub-samples.

Does the chain of custody have to be gapless?

The standard does not use the term but requires that identity and condition of the item remain traceable. Labs doing forensic, regulatory or safety testing typically need a gapless chain with holder, location and time for every change.

What should we do if an item arrives damaged?

Record condition and damage with photos, inform the customer before testing, and document their decision on whether to proceed. The test report then states the condition on receipt.

What happens to test items after testing?

The lab defines retention time and return or disposal, ideally at order acceptance. Both are documented as the final event of the chain.

Know where every test item is

TestLabIQ keeps receipt, handovers and location per test item in a gapless chain, with a scannable code and audit log.

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This guide is editorial orientation and not an interpretation of the standard. Always check the current standard text and the requirements of your accreditation body.