IMS Commercial Testing & Calibration Laboratories (GLP, ISO/IEC 17025, ISO 15189, ISO 9001)
IMS Commercial Testing & Calibration Laboratories (GLP, ISO/IEC 17025, ISO 15189, ISO 9001)
Every certificate a testing or calibration laboratory issues is a claim about a measurement, and this system is what makes that claim defensible.
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Written by practising auditors with 20+ years in the field.
By document type
| Category | Files |
|---|---|
| Manuals | 5 |
| Policies | 1 |
| Procedures & SOPs | 24 |
| Forms & Records | 28 |
| Checklists & Audit Tools | 7 |
| Registers, Logs & Matrices | 1 |
| Job Descriptions & Organisation | 1 |
| Training & Awareness | 2 |
| Guides & Work Instructions | 6 |
Key documents
| Reference | Document | Format |
|---|---|---|
| AGS-IMS-QM-01 | Integrated Management System Manual | Word |
| AGS-IMS-QP-08 | Methods Selection Verification and Validation | Word |
| AGS-IMS-QP-12 | Evaluation of Measurement Uncertainty | Word |
| AGS-IMS-QP-22 | GLP Study Management | Word |
| AGS-IMS-F-12 | Uncertainty Calculation Sheet | Word |
| AGS-IMS-F-15 | Four Year PT Plan and ILC Report | Word |
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Overview
An integrated management system for commercial testing and calibration laboratories serving industry, government and the public, built on ISO/IEC 17025 and reinforced by Good Laboratory Practice, ISO 15189 and ISO 9001. The manual carries the impartiality, confidentiality and competence policies, while a standards cross-reference matrix and a scope of activities document show an assessor how the schemes interlock and where each requirement is answered.
The technical core follows the work: method selection, verification and validation, metrological traceability, evaluation of measurement uncertainty with a worked calculation sheet, and decision rules governing statements of conformity. Validity of results rests on proficiency testing and interlaboratory comparison planning, retest analysis and control of nonconforming work. Equipment is held by history card, maintenance schedule and intermediate check, and a GLP study management procedure with a GLP to ISO/IEC 17025 bridge guide sets out where the two regimes agree and where they diverge.
What this system covers
- Method selection, verification and validation — proving the methods on your scope
- Metrological traceability and measurement uncertainty — traceability chains and uncertainty budgets
- Decision rules and statements of conformity — declaring a pass or fail against a specification
- Equipment control — acceptance, preventive maintenance, intermediate checks and equipment history
- Validity of results — proficiency testing, interlaboratory comparison and nonconforming work
- Facilities and environmental conditions — monitoring what influences a result
- Impartiality, confidentiality and competence — declarations, skill matrices and authorisation
- GLP study management — study conduct, report verification and the bridge to ISO/IEC 17025
Who it's for
Quality and technical managers in commercial testing and calibration laboratories, and the consultants who support them, usually at one of three moments: a first application for ISO/IEC 17025 accreditation, an extension of scope, or assessment findings that have to be closed. Everything is editable to your own test and calibration menu and equipment, so every clause an assessor raises has a named document behind it.
Everything you get
Every toolkit gives you a full set of working documents for your standard, ready to edit and use.
Native Microsoft files. Add your logo and adapt every document to how you work.
Your full toolkit arrives as a ZIP the moment payment clears.
One purchase covers everyone in your organisation. No per-seat fees.
Built by people who run real audits, so the content matches what assessors check.
One payment, perpetual licence for your organisation. No subscriptions, no renewals.
Full refund if your files are faulty, incomplete or not as described and we can't put it right
Frequently asked questions
What exactly do I receive?
A downloadable ZIP containing the full set of ready-to-use documents for this toolkit — manuals, procedures, forms, records, checklists, guidance and training material, all in editable Word and Excel format. The exact document count is shown at the top of this page.
Are the documents really editable?
Yes. Every file is native Microsoft Word or Excel — no locked PDFs. Add your logo, change wording, and tailor the content to your organisation. The toolkit is yours to keep and reuse.
Does this certify my organisation?
No. These are documentation toolkits aligned to the relevant standard to help you prepare. Certification itself is issued by an accredited certification body after their audit. Our toolkits give you a strong, audit-ready starting point.
How is it delivered?
Instantly and digitally. There's no physical shipment — you download the files right after payment and receive a backup link by email.
Do I get updates?
Yes. If we revise this toolkit, you're entitled to the updated version at no extra cost — just contact us with your order details.
What is your refund policy?
These are digital products, so once a toolkit has been downloaded we cannot take it back. If you have not downloaded yet, contact us and we will cancel the order and refund you in full. We also refund in full if the files are damaged, incomplete, or not what the product page described.
Cannot find your standard?
Tell us which scheme you work to. We will point you to the right toolkit.
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