Form · FRM-27
Proficiency Testing and ILC Plan and Participation Record
Four-year PT/ILC plan by scope area and the record and evaluation of each participation.
Purpose
Part A is the rolling four-year proficiency testing and interlaboratory comparison plan covering every scope area; Part B records each participation from registration to evaluation and action, per clause 7.7.2 and SOP-17.
What it covers
- Part A - Four-year plan
- Part B - Participation records
How to complete it
- 1.Part A: list every discipline, sub-discipline, range and technique in the scope; for each, plan at least one PT or ILC within the four-year cycle (and at least one per discipline per year), naming the scheme or comparison partner and the planned date; record justification for any area without a suitable scheme and the alternative (bilateral comparison).
- 2.Part B: for each participation record the scheme, provider accreditation, item, dates, engineer (routine staff), submitted results with uncertainty, reported performance (En / z), the Laboratory's evaluation against SOP-17 criteria, and actions (FRM-13 / FRM-08 numbers).
- 3.Review the plan at management review and update it after each round.
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-17
Ensuring the Validity of Results
Quality control, control charts, intermediate checks, proficiency testing and interlaboratory comparison programme.
- CHK-01
ISO/IEC 17025:2017 Gap Analysis and Self-Assessment
Clause-by-clause self-assessment with evidence, gap and action columns.
- FRM-01
Master Document Register
Register of every controlled internal and external document with revision, status and distribution.
- FRM-02
Document Change Request
Request, impact assessment and approval of a change to a controlled document.
- FRM-03
Records Retention Schedule and Disposal Log
Retention periods by record type and a log of authorised disposals.
- FRM-04
Internal Audit Programme and Audit Plan
Annual audit programme covering every clause and activity, plus the plan for a single audit.
- FRM-05
Internal Audit Checklist
Clause-by-clause question set with evidence and finding columns for auditing against ISO/IEC 17025.