ISO 17025 Certification In Saudi Arabia

We review your laboratory’s current practices against ISO 17025 requirements, identify gaps, and define the scope of testing or calibration activities. Common gaps include missing method validation, incomplete calibration records, or unclear technical responsibilities.

We develop customized documentation aligned with your laboratory operations, including:

• Quality manual
• Technical procedures and test methods
• Equipment and calibration records
• Forms, logs, and reports

Documentation reflects actual laboratory practices,not generic templates.

Laboratory personnel implement documented procedures in daily activities. We support:

• Technical and quality system implementation
• Staff awareness and competency training
• Practical alignment with ISO 17025 requirements

This stage is critical for audit success.

An internal audit is conducted to verify compliance and technical readiness. Nonconformities are addressed, and management reviews laboratory performance before the certification audit.

An accredited body conducts:

• Stage 1 Audit (system and documentation review)
• Stage 2 Audit (technical competence and implementation assessment)

After successful closure of findings, ISO 17025 certification or accreditation is granted. The approval is maintained through periodic surveillance or reassessment audits.