Greenlight Guru Medical Device Blog

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How Process Excellence Leads to Product Excellence - Featured Image

How Process Excellence Leads to Product Excellence

Today, we are talking to Mike Fisher, who is the director of product development at the Global Cente...
13 Common Pitfalls to Avoid During Medical Device Product Development - Featured Image

13 Common Pitfalls to Avoid During Medical Device Product Development

  Are you falling into some of the common traps that surround medical device product development?
Technical File vs. 510(k) vs. Design History File: What Medical Device Developer Should Know - Featured Image

Technical File vs. 510(k) vs. Design History File: What Medical Device Developer Should Know

Sometimes it feels like you need to know an entirely new language to work in the medical device fiel...
Best Practices for Expediting Your Medical Device Product Development - Featured Image

Best Practices for Expediting Your Medical Device Product Development

Speed to market is one of the major challenges for medical device companies; how can you expedite th...
Top 30 Medical Device Conferences You Should Be Attending in 2017 - Featured Image

Top 30 Medical Device Conferences You Should Be Attending in 2017

If you’re looking to land your company's next big deal, keep up on the latest regulatory trends, for...
Top 10 Most Popular Medical Device Articles of 2016 from greenlight.guru (Plus Top 5 Free Webinars and Podcasts) - Featured Image

Top 10 Most Popular Medical Device Articles of 2016 from greenlight.guru (Plus Top 5 Free Webinars and Podcasts)

Thanks for helping make 2016 another big and exciting year for greenlight.guru filled with growth! W...
Why Use ISO 14971 vs. FMEA (Template Included) - Featured Image

Why Use ISO 14971 vs. FMEA (Template Included)

This may be stating the obvious, but engineers are generally very analytical. One of the areas where...
Design History File (DHF) vs. Device Master Record (DMR) vs. Device History Record (DHR): Understanding the Differences and What Documents to Include - Featured Image

Design History File (DHF) vs. Device Master Record (DMR) vs. Device History Record (DHR): Understanding the Differences and What Documents to Include

DHF. DMR. DHR. It’s bad enough that medical device product development has a whole slew of new terms...
Recovery Force Accelerates Their Product Development Efforts Using greenlight.guru [Case Study] - Featured Image

Recovery Force Accelerates Their Product Development Efforts Using greenlight.guru [Case Study]

With its innovative technology in the highly competitive and expanding compression therapy market, i...
5 Medical Device Project Management Tips That Will Help You Complete Your Project On Time - Featured Image

5 Medical Device Project Management Tips That Will Help You Complete Your Project On Time

If you’re an engineer at a small medical device company, chances are, at some point, you’re going to...
Best Practices for an Effective Medical Device Design Transfer Process - Featured Image

Best Practices for an Effective Medical Device Design Transfer Process

With everything there is out there on the subject of Design Controls, you’d expect to find more on t...
Understanding Risk in Medical Device New Product Development (NPD) - Featured Image

Understanding Risk in Medical Device New Product Development (NPD)

Editor's Note: This is a guest post by Jeff Groh, President at New Product Visions and was originall...

The Greenlight Guru Medical Device Blog

Providing you actionable tips, best practices and insights for better medical device quality, compliance and product development.

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