Why product manufacturers should change their document-centric system

Engineering Departments Hold the Keys to Connected Data

Top 3 reasons why your PLM project is certain to fail before it has started

How to change skin, logo and favicon in Aras Innovator

If you cannot define your own requirements, you should not go out-of-the-box

Why you should centralize your product development data

How to fight the FIRE

The robots are coming to a shop floor near you!

The Big Lie of Pre-validated Systems

Dancing with the big guys

What we can learn from the European Spallation Source

What is Product Lifecycle Management? And what is it not

How PLM supports New Product Development & Introduction

PLM life is not without risk

Master Data Management and the continued battle for replacing spreadsheets

How PDM systems can manage specific CAD design data

Less than 25% of medical device manufacturers are ready to meet EU MDR deadline

How to Improve Product Development Processes

Medical Device Industry Trends For 2021

What is Minerva DevOps? Introducing our new product, Minerva DevOps

Stakeholder Engagement to Foster Effective Business Change

The 2021 State of Medical Device Product Manufacturing Survey

What are your (IT) New Year's resolutions?

7 Books that will help you understand digital transformation a bit better

Did you miss the virtual Aras Digital 2020 Europe Event?

Inspired by Carestream Health: How Minerva PLM for Medical Device contributes to smarter product innovation and improved user experience at the world class manufacturer

Why your traditional PLM is failing you

The evolution of PLM: Part 2

World Class Medical Device Manufacturers Trust Minerva

Why do More Than 30% of Digitalization Projects Succeed?

The COVID-19 crisis has given us tools. Now, we need to learn how to use them

Dude, Where’s Your Product Data?

Why Remote Work Will Be the New Normal for medical device manufacturers

Variant Management in Minerva PLM

You need automated document control, Mr. Skogen!

Are you ready for digital transformation?

Companies are still not good at defining requirements for their technology solution – and that is why their investments fail!

The value of traceability when working with regulation and documentation in the design process

Here is how you can save 15 hours on unproductive rework

How To Manage Product Design Documentation With A Connected Workflow

The importance of working Design Control procedure

Implementing an effective Risk Management process

Risk Management with Minerva PLM for Medical Device

Focusing on a product-centric approach is the path towards EU MDR compliance

EU MDR will be making life harder for small and medium medical device manufacturers

Ready for MDSAP? This is what you should know about the new regulatory change

IVD companies are in risk of being stuck in a traffic jam

Ready for the EU MDR? Here are 3 things you must do before the deadline

The lack of Notified Bodies puts medical device companies at risk of missing compliance deadline with EU MDR

The top 5 medical device trends for 2018 -Revisited

Why we developed Medical Device PLM...

Medical Device Digital Trends For 2018