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Request a Polarion Demo for 21 CFR 820

Key Aspects of FDA 21 CFR 820

  • Complete traceability of all artifacts

  • Traceability reports

  • Manage design documents and design controls

  • Approvals and escalations of complaints, non-conformances and defects

  • Faster audits

 

We get it.  Sometimes you are tired of looking at videos and want to see the solution directly and speak with a real person.

Send us your information and we'll schedule a demo within 2 days or find a time that fits your schedule.

No time like the present? Call us to schedule +1.248.247.0055.

+1.248.247.0055

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