Master Document List

Purpose

The Master Document List is the controlled index of every document in the pack as issued by ValiTrac (version 2.0, 2026-09-13). On adoption, the Laboratory transfers this list into FRM-01 Master Document Register, adds its own revision numbers, approvers, effective dates and review dates, and thereafter maintains FRM-01 as the live register. This list is retained as the record of what was received.

What is inside

3 sections, about 3 pages when printed.

1. 1. Purpose
2. 2. Document list
3. 3. Summary

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-01

  Control of Documents

  Creation, review, approval, issue, change and withdrawal of internal and external documents.

• 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.

• CHK-01

  ISO/IEC 17025:2017 Gap Analysis and Self-Assessment

  Clause-by-clause self-assessment with evidence, gap and action columns.

• GD-01

  Read Me First - How to Use and Customise This Pack

  Adoption roadmap, find-and-replace tokens, document hierarchy and a 12-week implementation plan.

• GD-02

  UKAS Accreditation Readiness Roadmap

  What happens from enquiry to grant of accreditation, what assessors sample, and how to clear findings.

• GD-03

  ISO/IEC 17025:2017 Clause Cross-Reference Matrix

  Every clause of the standard mapped to the manual section, procedure and records that address it.