Quality
How you follow specifications, inspections, traceability and nonconforming products.
ISO certification for manufacturing companies
From incoming materials to delivery, the system needs to work every day. We discuss production flows, people and records so the assessment reflects the way your factory operates.
Three areas to discuss
How you follow specifications, inspections, traceability and nonconforming products.
How you manage environmental aspects of production, from raw materials and consumption to waste.
How you identify hazards associated with work, equipment and maintenance activities.
The choice and availability of certification are confirmed for the requested activities, standard and scope. You do not need to select all three standards.
A starting situation
A useful conversation starts with the product, process stages and customer requirements. We clarify the activities in scope and how the assessment is planned, including shifts and outsourced operations. Management system certification is separate from product certification.
Preparing for an audit ↗What we clarify together
Receiving, manufacturing, inspection, storage and delivery, including outsourced processes.
Inspection records, batch identification where relevant, maintenance and nonconformity management.
Responsibilities, training, communication of changes and how results are reviewed.
Clarity from the first conversation
A useful proposal starts with your actual operations. Share a few details to start the conversation.
For a relevant proposal
Before you start
Updated on 16 October 2026.
ISO 9001 concerns the quality management system. A system certificate is not a conformity certificate for every product and does not replace product-specific assessments.
Yes. Shift arrangements and the activities performed are relevant to audit planning. Share these alongside headcount and locations so the proposal can reflect your operations.
References: ISO: certification · ISO 9001 · ISO 14001 · ISO 45001