Life Sciences

Keeping track of regulatory compliance and ensuring consistent and high product quality is key to your business. These can be time consuming processes. M-Files, allows for workflow automation - allowing the right staff access to the information instantly.

Life Sciences

Automate Quality Processes

M-Files can automate manual processes from change control to training and CAPAs, ensuring consistency and verifying your staff are following procedures.

Share procedures and in-date policies

Allow your business to access the right information with a single up to date version of each document, that’s always current.

Accessible Secure Content

Keep your files safe and share with relevant parties. The M-Files system will help save time and ensure permissions are current, by automatically maintaining who has access with metadata driven permissions.

Reduce Regulatory Risks

We can help your business stay compliant, from FDA 21 CFR Part 11 to ISO 9001. We can reduce risk and aid successful audits, by recording, automating and organizing multiple elements of your business.

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What's New With M-Files in 2018?


Our partners over at M-Files have further improved their offering, and have developed the metadata section of the M-Files platform, which is now updated for 2018.

To read up on the improved system here is the summary and transcript of the...

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