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Software for Medical Engineering Manufacturers

Industry leadership and niche expertise for the medical industry.

PLM, PDM, and DMS keeps processes flowing in medical engineering

In medical engineering, ensuring compliance with industry standards such as FDA Title 21 CFR Part 11 is business critical. It is essential to comply and document your compliance with these industry regulations and requirements. PRO.FILE automates many of these tasks and, among many other things, lets you:

Process control

PRO.FILE is able to control the complex development and approval processes associated with quality control in medical manufacturing. A product data backbone provides a foundation for the consolidation of product-related data and documents from across all departments and systems. The result is better compliance and process automation.

Capabilities

Get more done with a portfolio of medical engineering solutions on your side.

Our Medical Engineering solutions

Empowering Medical Engineering manufacturers, dealers, reps, and consultants to work together to simplify the sales process, reduce friction, and accelerate revenue.

PRO.FILE

Streamlining Medical Engineering Compliance with FDA Standards

Speedmaxx

Automate your ERP, CAD, and PDM systems in rule-based configuration processes and visualize your products live in 3D.

PROOM

Pioneering Secure and Compliant Project Collaboration

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Testimonials

We are a technology-driven company and for us, DMStec is the perfect approach to embrace the digitalization of document-heavy business processes. More so than any other vendor, PROCAD was able to meet all of our requirements.”

Marius Schönberger

Head of IT, Medtron AG