“All documents are in the right place, no more lost, missed, or not approved files. Automation reduces the time spent on some work.”
Our Customers
MedTech teams around the world use qmsWrapper to keep quality, product development, and regulatory evidence connected.
Used by teams building and supporting medical products around the world.






































Built for the realities
of quality work.
Independent reviews from people using qmsWrapper in their day-to-day work.
“The team is better organized, we saved a lot of money, and managing QMS is easy.”

From a paper-based QMS to a connected eQMS.
When The Wetling Company needed to update its Quality Management System to ISO 13485:2016, it also used the opportunity to move from paper to an online QMS.
“We felt that we had found both software that would likely serve us well and also a ‘true partner’ that could support us.”
Practical for today.
Ready for what
comes next.
Quality and regulatory workflows designed around the needs of medical device, SaMD, and IVD teams.
Documents, events, risk, training, design, and regulatory evidence can stay connected instead of living in separate silos.
AI-assisted workflows can reduce repetitive work while people remain responsible for the decisions that matter.
Start with what your organization needs and expand through Foundation, Lifecycle, and Vigilance as your needs develop.
See how qmsWrapper could work for your team.
Every MedTech company has different quality and regulatory needs. See how qmsWrapper can support the work you need to manage today and give your team a connected system that can expand as your products, processes, and responsibilities grow.
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