ISO consulting services, sequenced for certification.

Gap assessment & readiness review

A clause-by-clause review of how your current operation maps to ISO 9001, 14001, 45001, 17025, or any combination. Document review plus a structured site walkthrough produces a numbered gap register with severity ratings and a sequenced remediation plan.

• Documented gap register with clause references
• Severity classification (major / minor / observation)
• Sequenced remediation roadmap with effort estimates
• Realistic certification timeline by standard
• Briefing presentation for executive sponsors

Management system implementation

End-to-end design and rollout of an ISO-aligned management system. Manual, procedures, work instructions, and forms are co-authored with your process owners so the system reflects how your operation actually runs.

• Quality / EMS / OH&S manual aligned to the standard
• Documented procedures and work instructions
• Risk and opportunity register (clause 6.1)
• Objectives, KPIs, and measurement plan
• Document control structure and version system
• Records architecture and retention schedule

Internal audit programme

Independent internal audits conducted to ISO 19011 methodology. Findings are evidence-based, classified, and accompanied by recommended corrective actions. Annual audit programmes can be planned and executed on a retained basis.

• Annual internal audit programme & schedule
• Audit checklists tied to documented procedures
• Field audits with finding evidence captured
• Audit report classifying nonconformities
• Corrective action verification and closure

Supplier & second-party audit

Independent supplier audits — useful for procurement teams, contract manufacturers, or before onboarding a critical supplier. Conducted to client-defined criteria or to ISO clauses where appropriate.

• Audit plan and supplier-specific checklist
• On-site audit with evidence capture
• Supplier scoring against agreed criteria
• Risk-rated finding report for procurement
• Corrective action follow-up (optional)

Certification readiness & audit support

We prepare your organisation for the accredited certification body's Stage 1 and Stage 2 audits, attend on your behalf as a technical advisor, and lead nonconformity closure within the certifier's response window.

• Pre-certification mock audit
• Stage 1 documentation review prep
• Stage 2 on-site audit support
• Nonconformity response & root-cause investigation
• Corrective action submission and closure

Surveillance & integrated management

Ongoing support through the three-year certification cycle. Quarterly check-ins, management review facilitation, internal auditor refreshers, and integration of multiple ISO standards into a single management system.

• Annual surveillance audit preparation
• Management review agenda & facilitation
• Continual improvement programme
• Integration of QMS / EMS / OH&S into IMS
• Recertification preparation (year three)

Laboratory accreditation (ISO/IEC 17025)

For testing and calibration laboratories: technical procedures, method validation, measurement uncertainty estimation, traceability mapping, internal quality control, and proficiency-testing planning.

• Quality manual aligned to ISO/IEC 17025
• Method validation files for in-scope methods
• Measurement uncertainty budgets
• Calibration & traceability register
• Internal QC and PT participation plan

Industrial / API-oriented compliance

For industrial clients with mechanical integrity, pressure-system, and materials-qualification obligations: technical document support, integrated quality controls, and audit-ready records aligned with both ISO 9001 and sector-specific (API-style) requirements.

• Materials qualification & traceability records
• Mechanical integrity programme support
• Reliability-engineering input to FMEA / risk
• Inspection & test plan (ITP) authoring
• Procurement and supplier qualification records