Advantages of certification to ISO 9001:2015 QMS

There are many good reasons for an ISO 9001 certification:

  • Cost and time saving
  • Increased process reliability within the company
  • Definition and documentation for increasing legal certainty and efficiency
  • Verifiable compliance with customer requirements
  • Increased competitiveness
  • Increased market acceptance

How long is the certification valid?

The company certificate is valid for three years and must be confirmed every year by a monitoring audit. A recertification is performed after three years.

ISO 9001:2015 
Quality Management

ISO 9001 is the most widespread standard in the field of quality management and is internationally recognized. It defines the minimum requirements of an effective quality management system (QMS).

Ensure quality through process optimization

In order to prevail in the face of global competition, high, consistent quality, customer satisfaction and well-functioning processes are essential. To meet these requirements, a reliable quality management system is needed. The quality management standard ISO 9001:2015 provides the basis for this, outlining the minimum requirements that a quality management system has to fulfill.

Introducing ISO 9001 not only enables you to improve the performance of your company in all areas, but also demonstrates your company’s high quality standards to internal and external stakeholders.

Process of certification to ISO 9001:2015 QMS

Stage 1: Readiness assessment

The certification begins with a readiness assessment. During this, the audit team determines which requirements of ISO 9001 are already met and where improvements are required.

Stage 2: Audit

The readiness assessment is followed by the actual certification to ISO 9001:2015 audit. The audit is divided into a documentation/process check and an on-site audit. In the first step, the auditor checks the documentation (process descriptions), focusing on compliance with the requirements set out in the standard. The second step takes place on the company’s premises. Here, the effectiveness of the QMS and the implementation of the requirements of ISO 9001 are checked and assessed. Deviations discovered during the audit can be corrected. Once the auditors have checked and approved the effectiveness of the corrective measures, you receive an audit report and, once the process has been approved, the certificate.

As part of the certification procedure – consisting of a readiness assessment and document inspection in advance and a subsequent on-site company audit – the following elements, among others, are tested and assessed:

  • Context of the organization with specification of application area
  • Management/policy
  • Planning
  • Support
  • Operational realization
  • Assessment of performance
  • Improvement
  • QMS 9001 Internal Auditor
  • QMS 9001 Lead Auditor
  • EMS 14001 Internal Auditor
  • EMS 14001 Lead Auditor
  • OHSMS 45001 Internal Auditor
  • OHSMS 45001 Lead Auditor
  • MD QMS 9001 Internal Auditor
  • BCMS ISO 22301 Internal Auditor
  • EnMS ISO 50001 Lead Auditor
  • FSMS ISO 22000 Lead Auditor
  • IATF 16949 Automotive QMS Lead Auditor
  • ISMS ISO 27001 Internal Auditor

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