KubitDocs · Legislation

ISO 9001:2015 — Quality management systems. Requirements

Provisions the documents cite: clauses 8.5.1, 8.6, 8.7 and 10.2

What it requires

8.5.1 — production under controlled conditions, including monitoring and measurement at appropriate stages to verify that criteria for control have been met. 8.6 — planned arrangements are implemented to verify product requirements are met before release; documented information retains evidence of conformity with the acceptance criteria and traceability to the person authorising release. 8.7 — nonconforming outputs are identified and controlled; documented information describes the nonconformity, the actions taken, any concessions and the authority deciding them. 10.2 — nonconformity and corrective action.

How this entry is kept current

  • Citation status: carried from drafting; a source check is in the monthly scan queue.
  • Watched by: manual check each scan.
  • Automated scan: no public page to watch; checked by hand in the monthly review.

Every source is re-checked monthly and the result is published in the scan log. A change that alters what a document should say raises a revision, and past buyers of that document are told.

The 55 documents that cite it

Every KubitDocs document prints its statutory basis on the form itself, so the person signing can verify the citation rather than take our word for it.

CAS evidence records

Close-out records

Company policies

Inspection and test plans

Quality system documents