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.

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

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