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qmsWrapper

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61 reviews
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4.5
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qmsWrapper Reviews

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Verified User in E-Learning
UE
Verified User in E-Learning
01/31/2024
Validated Reviewer
Review source: Organic

Faster Audits, Better Traceability!

We've successfully cut on-site audit duration by over 50% by granting auditors the ability to examine documents within qmsWrapper. The inherent value lies in the traceability established between design controls and risk elements.
Emma F.
EF
Emma F.
Quality Management Specialist at Medical.CA
01/22/2024
Validated Reviewer
Verified Current User
Review source: Organic

The best eQMS for MedDev companies with a great Team!

It is a perfect software for startups and companies that wants to stop with paper-based and switch to eQMS. My favorite is their DMS and Traceability Matrix. The software has some of the remarkable QMS solutions for the medical device industry.
Sonja R.
SR
Sonja R.
11/20/2023
Validated Reviewer
Verified Current User
Review source: Organic

Overall, good software

I like that they offer ready-made templates that we can also change according to our requirements. Forms are easy to use, and thus reports are easy to create. I especially like the fact that before using the form, it must be approved by the responsible person, so that forms that have not been checked cannot be included in the system.

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HQ Location:
Toronto, Ontario

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@qmsWrapper

What is qmsWrapper?

qmsWrapper is a comprehensive quality management software designed specifically for medical device manufacturers and companies regulated by the FDA. The platform aims to streamline and enhance the effectiveness of quality management systems (QMS) by integrating project management, document control, risk management, and ISO 13485 compliance processes within a single framework. qmsWrapper's user-friendly interface and modular design make it adaptable to the needs of businesses of various sizes, from startups to established enterprises. With features like traceability, collaboration tools, and built-in compliance pathways, qmsWrapper helps organizations manage their quality processes more efficiently, ensuring compliance with relevant regulations while supporting the goal of delivering safe and effective medical devices to market.

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