Medical Device QMS Consulting

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Maximize Quality.

Minimize Burden.

Establish

At EnGenius, we create QMS procedures tailored to your business and product(s) such that quality and compliance are achieved in the least burdensome manner.

Improve

Every QMS needs to adjust to the evolving business needs and product revisions. Otherwise, it is only a matter of time before it proves suboptimal. EnGenius can help your business review and optimize existing QMS procedures in order to improve quality, streamline processes, and lower overall costs.

Support

The work of QMS never stops. Whether you have an unanticipated staff shortage due to employee turnover or are experiencing a temporary increase in workload, EnGenius can support meeting your existing QMS requirements.

Audit

Compliance is a cornerstone of every functional QMS such that regular internal audits are management system requirements. Whether you need a formal internal audit or just prefer to have an assessment of your system’s compliance risks, EnGenius can help with the applicable regulations and standards including:

  • ISO 13485:2016

  • ISO 14971:2019

  • ISO 62366-1:2015

  • ISO 62304:2006+A1:2015

  • ISO 82304-1:2016

  • ISO 14155:2020

  • FDA 21 CFR 820

  • FDA 21 CFR Part 11

  • EU MDR 2017/45

Contact Us

Whether you need support for the daily tasks or want us to revolutionize your QMS, it all starts with the first contact. Drop us a line!

ashkon@engeniussolutions.com
(657) 200-1550

555 Anton Blvd, STE 150
Costa Mesa, CA, 92626