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Ensure Compliance and Control

Medical devices require accuracy and oversight; we provide both with PLM solutions. 
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In the medical engineering industry, adherence to regulations, precision, and innovation are paramount to success. We offer an integrated suite of solutions, from Product Lifecycle Management (PLM), tailored to meet the unique needs of medical device manufacturers and engineering firms.

Meet Requirements with Medical Device PLM

Ensuring and documenting compliance with industry standards, such as FDA Title 21 CFR Part 11, is critical. PRO.FILE, our PLM solution, automates many of these tasks so you can:

Centralize data management

Maintain visibility and control the exchange of project documents with DMStec, our document management system, to promote consistency and dependability.

Gather virtual teams

PROOM provides secure project rooms where manufacturers, dealers, reps, and consultants can work together to simplify the sales process, reduce friction, and accelerate revenue—without the hassle of emails or FTP servers.

Track changes

Implement robust, system-based audit trails you can refer to in the future.

Automate processes

DMStec seamlessly creates file folders needed to obtain approvals and standardizes the electronic documentation of digital signatures and workflows.

Optical Machinery

From lasers to lenses, our solutions help optics companies manage complex product lifecycles, streamline sales processes, and enhance design accuracy with:

  • Improved equipment design: Create detailed plans that meet the specific needs of your applications.
  • Enhanced operational efficiency: Streamline the development and deployment of equipment to reduce lead times and improve efficiency.
  • Increased safety: Adhere to standards and regulations to lessen the risk of accidents and promote an injury-free workplace.

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

Need More Information?

Ready to standardize processes to ensure compliance?
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