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See Arena in Action
Get Compliant Products to Market Fast
Simplify compliance, reduce audit risks, and launch cutting-edge products fast.
Arena manages and documents corrective and preventive actions from end to end, helping you resolve issues and improve products with ease.
Streamline Your CAPA Workflows
Cloud-native QMS software, purpose-built for Life Sciences and Aerospace
Accelerate Issue Resolution
Leverage closed-loop processes to enhance visibility of quality concerns in context of the entire product record and speed issue resolution.
QMS
Streamline Document Management
Control and track product, quality, and training records in a single system.
Product-Centric Quality Management System
A single platform that connects quality processes, training records, and compliance evidence to the product record for full traceability throughout NPDI.
SINGLE SOURCE OF TRUTH
Simplify Regulatory Compliance
Ensure product and process compliance with global directives including FDA, EU MDR, ISO, and AS9100.
Centralize product and quality information to eliminate errors and launch faster.
Boost Traceability and Guarantee Compliance
Connect With the Systems You Rely On
Connect to 100+ no-code integrations, purpose-built for Arena.
ARENA ANALYTICS
Track KPIs to Enhance Product Quality
Review your active quality processes at a glance to identify unresolved issues and measure progress over time.
READY-TO-USE TEMPLATES
CUSTOMIZABLE DASHBOARDS
“Arena QMS is a true lifecycle management system that is better than the typical document-focused QMS solutions. Being able to manage BOMs and changes along with quality processes is a major advantage.”
Sanjay Banerjee, COO, Accuryn Medical
MEDICAL DEVICES
"Arena’s connected quality management approach helps us stay on track with meeting our product development milestones. We’re able to gain a snapshot of our progress at any given time with just a few clicks. It’s truly a game-changer!”
Angie Swanson, Lead Quality Engineer, NanoDx™, Inc.
BIOTECHNOLOGY
Product-Centric Quality Management System
A single platform that connects quality processes, training records, and compliance evidence to the product record for full traceability throughout NPDI.
SINGLE SOURCE OF TRUTH
Accelerate Issue Resolution
Leverage closed-loop processes to enhance visibility of quality concerns in context of the entire product record and speed issue resolution.
Centralize product and quality information to streamline collaboration and speed corrective action.
Centralize Workflows
Enable Global Collaboration
Connect internal engineering and quality teams with supply chain partners to identify and resolve quality issues in record time.
Automate Document Management
Control and track product, quality, and training records in a single system so you're always audit-ready.
Simplify Regulatory Compliance
Ensure product and process compliance with global directives including FDA, EU MDR, ISO, and AS9100.
Track quality documents and processes with ease to ensure products comply with global regulations.
Guarantee Product Compliance
Get Compliant Products to Market Fast
Simplify compliance, reduce audit risks, and launch cutting-edge products fast.
QMS
