Procedure · SOP-10
Facilities and Environmental Conditions
Specifying, monitoring, controlling and recording the environmental conditions that affect results.
Purpose
To define how the Laboratory specifies, achieves, monitors, controls and records the facilities and environmental conditions necessary for the valid performance of its calibrations, and how it acts when conditions fall outside limits.
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.
- –Environmental monitoring data and weekly review
- –Excursion records and impact evaluations
- –Environmental readings per job
- –On-site conditions
- –Building services maintenance records
- –Post-change environmental surveys
What an assessor looks for
The document closes with these points, so you can check your own practice before someone else does.
- –Reading the logger data for the day of a sampled certificate and checking the worksheet readings agree.
- –Confirming the monitoring sensor is calibrated, positioned sensibly and that its uncertainty is adequate for the limit.
- –Asking what happens when the air-conditioning fails, and looking for the evidence of what actually happened last time.
- –Checking that on-site conditions were recorded and within limits.
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-32
On-Site Calibration at Customer Premises
Planning, environmental control, equipment transport and records for calibrations performed away from the laboratory.
- FRM-17
Environmental Monitoring Log
Record of temperature, humidity and other environmental conditions against limits.
- FRM-47
On-Site Work Record
Environmental conditions, equipment used and transport checks for work at customer premises.
- 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.
- SOP-03
Internal Audit
Planning, conducting, reporting and following up internal audits of the management system and technical activities.