RESOURCES
Everything you need
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RESOURCE LIBRARY
The Arena resource library includes a collection of articles, white papers, guides, tips, tools, templates, and ebooks focused on product lifecycle and quality management. This library provides educational and best practice insights for product design, quality, manufacturing, and supply chain teams.
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ARTICLES
Your one-stop-shop for news, best practices, and helpful information geared just for you.
Tips, Tools, and Events
Check out our complete resource library to view events, webinars, briefs, and helpful guides.
Best Practice Articles By Topic
Top Resources
NEW ERA INNOVATION
This report is based on a series of interviews with senior leaders at six leading-edge organizations in healthcare, consumer electronics, and autonomous vehicle technologies. Learn how new technologies are changing the face of product innovation.
HOW TO BUY GUIDE
This software buyer’s guide is designed to help you buy the right software for any business need—from product development and quality processes to manufacturing operations, finance, design, and digital marketing.
PRODUCT INNOVATION
As companies pick up the pace of innovation to meet customer demand, they need to reduce costs and ensure regulatory compliance to stay ahead of increased global competition. Learn how to accelerate your product launch processes.
BOM MANAGEMENT
Working with dispersed teams and supply chain partners requires collaboration around the latest bill of materials (BOM) to reduce production errors and shipping delays. Learn how Arena provides a more intelligent way manage your BOMs.
7 PRINCIPLES OF QMS
For medical device companies, having a rock-solid approach to quality is a prerequisite for success and innovation. Read this eBook to learn how to overcome process delays, compliance risks, and barriers that impede innovation.
REMOTE AUDITS
Our panel discussion with Morey Corporation, Hyalex, and Arena’s Security Engineering Director uncovers best practices to ensure audit-readiness for FDA, ISO, Export Controls, and other types of audits.
5 TIPS TO PASS AUDITS
An FDA or ISO audit is a potentially difficult part of doing business. Arena enables medical device manufacturers of Class I, II, and III devices to address FDA regulations 21 CFR Part 11, 21 CFR Part 820, and ISO 13485 requirements.
COST OF MISTAKES
A single mistake can delay your next product launch and cost millions. This calculator includes visible costs such as team expenses along with strategic cost impact from lost market opportunities and customer dissatisfaction. See what mistakes are costing you.