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How to reach compliance on REACH and RoHs
How to efficiently detect conflict minerals in your products
Why Risk Management is a company-wide responsibility
Why is configuration management so difficult?
Medical device manufacturers are greatly challenged by the burden of increasing regulatory demands
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
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
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