Welcome to Audveria

Audveria is a modern quality management system designed specifically for medical device and pharmaceutical companies. In this guide, we'll walk you through setting up your first inspection workflow.

Why Choose Audveria?

Medical device compliance is complex. Regulations like ISO 13485, 21 CFR Part 11, and EU MDR require careful documentation and traceability. Audveria simplifies this by providing:

Smart Checklists: Configure inspection templates for different product types
AQL Sampling: Automatic sample size calculations based on ISO 2859-1
Complete Audit Trail: Every action is logged for regulatory compliance

Setting Up Your First Workflow

Step 1: Create Inspection Templates

Navigate to Settings → Inspection Templates to create your first template. You can enable or disable specific checklist items based on your needs:

Logistics checks (quantity, packaging, seals)
Medical device specific checks (CE marking, UDI, sterile barriers)

Step 2: Configure Receiving Locations

Set up your warehouse locations to track where shipments are received and inspected.

Step 3: Start Inspecting

When a shipment arrives, create a new shipment record, complete the gate check, and proceed to item-level inspection.

What's Next?

Stay tuned for more guides on advanced features like NC case management, multi-site deployments, and integration with your existing ERP systems.

Have questions? Reach out to us at contact@audveria.com.