Industry leadership and niche expertise for the medical industry.
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:
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.
Get more done with a portfolio of medical engineering solutions on your side.
Empowering Medical Engineering manufacturers, dealers, reps, and consultants to work together to simplify the sales process, reduce friction, and accelerate revenue.