RESOURCES
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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.
Tools and Events
Get access to our on-demand webinars, product briefs, and helpful tools and templates.
Industry Guides
Get in-depth information on what’s happening in the industry and how Arena makes an impact. Read our industry guides and related resources.
Best Practice Articles By Topic
Top Resources
PRODUCT 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.
EMBRACE A NEW ERA
Cloud-native solutions drive agile processes and real-time collaboration. We explore how cloud-native solutions provide manufacturers a more agile framework to efficiently execute product work and accelerate innovation.
EV COMMERCIALIZATION
A guide for electric vehicle innovators. To achieve new product development and introduction (NPDI) success, EV manufacturers must have the wherewithal to quickly adapt and overcome these obstacles.
THRIVE ANYTIME
We explore how the adoption of enterprise cloud-based PLM and QMS solutions and other technologies enable product manufacturers to quickly adapt to change and make the necessary digital transformation to compete in today’s global economy.
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.