Procedure · SOP-30
Intermediate Checks of Reference Standards and Equipment
Checks between calibrations that maintain confidence in the calibration status of reference standards.
Purpose
To define the intermediate checks performed on reference standards, working standards and critical equipment between calibrations, so that confidence in their calibration status is maintained, drift or damage is detected before it affects reported results, and the extent of any impact can be bounded.
What is inside
10 sections, about 3 pages when printed.
- 1. Purpose
- 2. Scope
- 3. References
- 4. Definitions
- 5. Responsibilities
- 6. Procedure
- Records generated by this procedure
- Monitoring and performance indicators
- Assessment readiness notes
- Related documents
Records it generates
Applying this procedure produces the following records, which are the evidence an assessor samples.
- –Intermediate check plan per item
- –Intermediate check records
- –Control charts of check values
- –Transport checks
- –Failure investigations
What an assessor looks for
The document closes with these points, so you can check your own practice before someone else does.
- –Asking to see the ice-point check for the PRT on the day of the sampled certificate.
- –Checking check limits are derived from the budget and the item's tolerance, not arbitrary.
- –Reviewing the trend chart for the calibrator's 10 V check.
- –Confirming before-and-after transport checks for an on-site job.
Before you use it
- Replace every square-bracket token, starting with [LABORATORY NAME], [ADDRESS] and [EFFECTIVE DATE]. The full token list is in GD-01 Read Me First.
- Have the content technically reviewed against how your laboratory actually works, then approved by the responsible manager before it becomes a controlled document.
- Update the Word fields after editing so the table of contents and page numbers are correct: select all, then press F9.
- Record the document in your own document register and set its review date.
- Delete the assessment readiness notes if you do not want them in your controlled version; they are guidance for you, not requirements.
Related documents
- QM-01
Quality Manual
Top-level description of the management system against every clause of ISO/IEC 17025:2017.
- SOP-11
Equipment Selection, Calibration and Maintenance
Equipment lifecycle: selection, acceptance, identification, calibration programme, labelling, maintenance and disposal.
- SOP-17
Ensuring the Validity of Results
Quality control, control charts, intermediate checks, proficiency testing and interlaboratory comparison programme.
- FRM-28
Quality Control Chart Log
Check-standard results plotted against warning and action limits, with trend review.
- FRM-35
Intermediate Check Record
Result of a check between calibrations against defined acceptance limits.
- CHK-01
ISO/IEC 17025:2017 Gap Analysis and Self-Assessment
Clause-by-clause self-assessment with evidence, gap and action columns.
- SOP-01
Control of Documents
Creation, review, approval, issue, change and withdrawal of internal and external documents.
- SOP-02
Control of Records and Technical Records
Identification, storage, protection, retention, amendment and disposal of quality and technical records.