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Auditing services

Improve your quality management system with our internal auditing services for medical device manufacturers.

Auditing services for medical devices industry

We develop effective yearly audit plans that turn auditing into an effective tool, not just a mandatory requirement.

Internal audits

Internal audits are part of the continuous improvement of the QMS and are mandatory. They identify gaps and the effectiveness of your quality management system. Internal audits give you confidence that regulatory requirements are accurately implemented in your processes.

We view internal audits as ways to improve rather than solely for compliancy to get the most of out of your QMS.

  • full ISO 13485 QMS audit
  • partial ISO 13485 audit, such as only management responsibility
  • full or partial ISO 9001 audit
  • full or partial ISO 13485+9001 audit
  • full or partial ISO 13485 audit + MDR/IVDR 
  • full or partial ISO 13485 audit with emphasis on applicable standards such as IEC 62304 or IEC 62366.

Medical Device Single Audit Program (MDSAP) mock audits

MDSAP is a program where with a single audit, up to 5 country QMS requirements for Australia, Brazil, Canada, Japan and USA can be satisfied. The MDSAP requirements are based on ISO 13485 and complemented with country specific requirements. Canada accepts only MDSAP quality management system certificates.

We perform mock audits, which will determine your readiness for an actual MDSAP audit.

Supplier audits

The quality of the materials or components you use in your medical device are a prerequisite for the quality of your product. Suppliers need a control method to ensure their operations are at the desired level.

A supplier audit is the most effective way to ensure that your suppliers comply with applicable standards and regulations, as well as your needs. We can audit your candidate suppliers before you approve it and take care of the follow-up audits.

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How can we help?

An auditor provides new insights to your quality management system, we can cover: ISO 13485:2016

  • ISO 9001:2015
  • MDR 2017/745
  • IVDR 2017/746
  • FDA QSR
  • MDSAP
  • Additional weightings for standards

Contact us for more information

Meeri Säily
Meeri Säily
Sales Director, Consulting and Clinical Trials

Explore our services

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Quality Management System ISO 13485

Setting up quality management systems (QMS) for medical device manufacturers.
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US FDA 21 CFR Title 820 (QSR)

We know quality systems, including the USA Food and Drug Administration Quality System Regulation, QSR, 21 CFR Title 820.

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QMS Improvement and Gap Analysis

Improvement of medical device manufacturer’s quality management system (QMS) and GAP analysis.

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