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Become a Certified Medical Device Quality Engineering Pro

A step-by-step video curriculum and mentoring program that turns regulatory complexity into a clear, repeatable quality system for any medical-device manufacturer.

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4.9/5 star reviews

Here's what you get:

Instant streaming access to 40+ HD training videos, transcripts, and slide decks.
Downloadable SOPs, forms, and templates (ISO 13485 QMS, risk files, validation protocols).
Monthly live group mentoring calls and a private Slack community for Q&A.
Lifetime updates reflecting new FDA guidance, EU MDR amendments, and standard revisions.

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$97 one time

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STILL NOT SURE?

Satisfaction guarantee

We want you to find value in our trainings! We offer full refunds within 30 days. With all of our valuable video training, we are confident you WILL love it!

STILL GOT QUESTIONS?

Frequently Asked Questions

Do you cover EU MDR, IVDR, and other global regulations?

Absolutely. Every module cross-references FDA, EU MDR/IVDR, ISO 13485, and MDSAP so you can comply worldwide.

What experience level is required?

The program starts with the basics for new quality engineers and quickly scales to advanced topics valuable for seasoned professionals and directors.

How is the mentoring delivered?

You receive monthly live group calls, on-demand replays, and 12-month email access for personalized feedback on your documents.