Supplier Audits
On-site quality system, process and product audits at suppliers and contract manufacturers.
Independent supplier and third-party audits by certified lead auditors — with defensible reports and closed-loop findings you can share with customers, regulators and boards.
Second-party audits assess your suppliers and contract manufacturers; third-party audits assess your own organisation on behalf of a customer or independent stakeholder. Both are conducted per ISO 19011 by lead auditors independent of the audited party.
We plan the audit against your criteria, run opening and closing meetings, gather objective evidence, classify findings and issue a defensible report. Where required, we verify corrective actions to closure so findings actually drive improvement — not just paperwork.
On-site quality system, process and product audits at suppliers and contract manufacturers.
Third-party audits performed on your organisation on behalf of a customer or stakeholder.
Independent mock audits against ISO 9001, API Q1/Q2, AS9100 or IATF 16949 before your certification body arrives.
Layered process audits and product audits verifying conformance at the point of manufacture.
Classified findings (major, minor, opportunity), root-cause guidance and independent CAPA verification.
Multi-year supplier audit programmes with risk-based scheduling and dashboarded reporting.
Every audit follows the same discipline: agreed criteria, objective evidence, classified findings and verified corrective action.
Agree scope, criteria and audit plan; nominate independent lead auditor and technical experts.
Opening meeting, evidence-based fieldwork, daily briefings and closing meeting.
Classified findings with objective evidence and a defensible written audit report.
Review CAPA responses, verify effectiveness and issue closure statement.
Delivered across North America, with India and the UAE coming soon.
A second-party audit is performed on your suppliers by you (or an agent acting for you). A third-party audit is performed by an independent body — either a certification body granting a certificate, or an independent firm reporting on your behalf to a customer or regulator.
Yes. Our lead auditors hold IRCA, Exemplar Global or equivalent registration against the standards audited (ISO 9001, API Q1/Q2, AS9100, IATF 16949, ISO 14001, ISO 45001) and meet the ISO 19011 competency criteria for third-party audit teams.
Yes — including API Q1 and Q2 (oil & gas), AS9100 (aerospace), IATF 16949 (automotive), ISO 13485 (medical devices), ISO 14001, ISO 45001 and ISO 27001.
Yes. We design and operate multi-year, risk-based supplier audit programmes with tiered supplier segmentation, standard checklists, dashboards and CAPA verification.
We audit across North America from our Mississauga (Ontario) and Austin (Texas) offices, with additional coverage in India and the UAE coming soon.
Send us the scope and criteria — we'll assemble the lead auditor and technical team within one business day.