essential guide eu mdr compliance

The Essential Guide to EU MDR Compliance

Expert guide overview

Do you have a set roadmap for certifying your devices under the new European Union (EU) Medical Device Regulation (MDR)? If you currently market and sell medical devices in the European Economic Area (EAA) or are planning to do so in the near future—now is the time to put the proper measures and systems in place to ensure compliance.

You will learn:

Important dates for the MDR transition
The MDR requirements that will have the greatest impact on your quality management processes and product portfolio
Key steps for a successful MDR implementation
How an enterprise quality management system (eQMS) can help simplify compliance

What we do

New product development (NPD) and new product introduction (NPI) practices have shifted over the last decade as companies have picked up the pace of innovation. Developing products with more electronics, software, and sensors requires keeping internal teams and external supply chains on the same page throughout the entire product lifecycle. Read this white paper to learn how to overcome barriers to product innovation and streamline your product development and launch processes.

How we deliver value

Competition is increasing at light-speed and products are becoming more complex as they connect devices, people, and systems. This requires solutions scale with your requirements. Arena PLM eliminates communication barriers, recuces costs, and increases profitability so you can deliver high-quality products to market fast.

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1,300 Global Customers

"We get terrific feedback from the give and take of the review process. Indeed, partners have provided feedback that helped us avoid making unnecessary, confusing, or costly changes."

David Sangster | Senior VP of Operations, Nutanix