Form · FRM-29
Calibration Certificate Template
Certificate layout containing every element required by clause 7.8.2 and 7.8.4.
Purpose
The layout for calibration certificates, containing every element required by ISO/IEC 17025 clauses 7.8.2 and 7.8.4, the Laboratory's standard statements (SOP-18 section 6.3), the reference standards table, the results tables, the decision rule section and the authorisation block. The template is implemented in the certificate generation system; this document is the controlled specification of its content.
What it covers
- Header (every page)
- Section 1 - Identification
- Section 2 - Conditions and reference standards
- Section 3 - Results
- Section 4 - Statement of conformity (only where requested and agreed)
- Section 5 - Remarks, deviations, opinions and interpretations
- Section 6 - Standard statements
- Section 7 - Authorisation
How to complete it
- 1.Populate every field from the worksheet and job file; never type results directly from memory.
- 2.Use the standard statements verbatim; alterations require Technical Manager approval.
- 3.For accredited work include the accreditation symbol and number in the header and identify any non-accredited result with an asterisk and the standard statement; omit the symbol entirely for non-accredited certificates.
- 4.State the sign convention (correction or error) once and use it consistently.
- 5.Include 'End of certificate' after the last item of content and page X of Y on every page.
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.
Related documents
- QM-01
Quality Manual
Top-level description of the management system against every clause of ISO/IEC 17025:2017.
- SOP-18
Reporting of Results and Calibration Certificates
Content, review, authorisation, issue and amendment of certificates and reports, including opinions and interpretations.
- SOP-29
Decision Rules and Statements of Conformity
Selecting, agreeing, applying and reporting decision rules, guard bands and conformity statements.
- SOP-31
Use of the Accreditation Symbol and Reference to Accreditation
Rules for using the accreditation body's symbol and claiming accredited status on certificates and marketing.
- FRM-48
Certificate Amendment and Reissue Record
Control of amended, reissued or withdrawn certificates.
- CHK-01
ISO/IEC 17025:2017 Gap Analysis and Self-Assessment
Clause-by-clause self-assessment with evidence, gap and action columns.
- CHK-03
Calibration Certificate Review Checklist
Review gate for every certificate before authorisation and issue.
- FRM-01
Master Document Register
Register of every controlled internal and external document with revision, status and distribution.