Request a Polarion Demo for 21 CFR 820
Key Aspects of FDA 21 CFR 820
Complete traceability of all artifacts
Manage design documents and design controls
Approvals and escalations of complaints, non-conformances and defects
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.