You've got high standards. Maintaining regulatory compliance and ensuring product quality consistency are your top priorities. Tracking quality processes and verifying completion can be extremely time consuming. M-Files automates workflows while allowing the right people to access the right information instantly.


Disseminate up-to-date policies and procedures

What if everyone in your organization could find the right information quickly? In M-Files, there’s only one version of every document. No matter what type of quality document is needed, it’s always current.

Automate quality processes

Your company depends on you to keep things under control. You need to ensure specific procedures are followed, but you shouldn’t have to manually manage day-to-day processes’-Files automates quality workflows like change control, CAPAs and training. That means you can ensure consistency while M-Files verifies that everyone is following procedures.

Keep track of critical tasks

You’ve identified something that needs to be changed and created a new procedure. That’s great. But how do you verify that the correction was implemented? M-Files keeps track of all required activities and assignments to make sure your fix is being implemented.

Reduce regulatory risk

Failing to comply with regulations is expensive and risky. From ISO 9001 to FDA 21 CFR Part 11, our job is to help you stay compliant. M-Files helps reduce the risk of unsatisfactory audits and regulatory non-conformance by organizing, recording and automating everything in your business.

Mobile Access - eSigning Demonstration

M-Files Mobile Access enables businesses in highly regulated industries to maintain compliance outside of the office. The eSignature capability integrated into M-Files allows businesses to approve and monitor processes associated with regulations such as FDA 21 CFR Part 11 and EU GMP Annex 11...even from a mobile device.