Filter All Blog Posts

About the Author

Nick Tippmann is an experienced marketing professional lauded by colleagues, peers, and medical device professionals alike for his strategic contributions to Greenlight Guru from the time of the company’s inception. Previous to Greenlight Guru, he co-founded and led a media and event production company that was later acquired.

Showing Results for

Product Development

Why Usability Matters

November 24, 2021
Usability is essential. If you design something, anything used by humans, it needs to be designed for the users. This is especially true for medical devices. Read More
Product Development

A Special Glimpse into Medtronic's Recent Developments in Spine & Biologics Technology

November 17, 2021
Do you want to alleviate pain, restore health, and extend patients’ lifespan? Accelerate the transformation of the spine industry by making outcomes and technologies... Read More
Regulatory Submission

What are the Top Compliance Issues Plaguing Medical Device Manufacturers?

November 10, 2021
Medical device companies must comply with a list of strict requirements throughout the duration of their product's lifecycle. These compliance efforts will be put to the test... Read More
Establishing a QMS

Greenlight Guru and Formlabs Partner to Mitigate Risk and Accelerate Product Development in order to Improve Patient Outcomes

November 9, 2021
Customers benefit from leveraging industry medical specific eQMS and 3D printing Read More
Product Development

Setting the Record Straight on Usability & Human Factors

November 3, 2021
What is usability? Human factors? Are they one and the same or different in the medical device industry? When do each apply? Whatever you call it, both are very important... Read More
Product Development

Project Management for Product Development of Medical Devices

October 27, 2021
How should you approach project management for medical device product development ? Stop managing your projects using methods and tools that delay timelines and increase... Read More
Regulatory Submission

Assessing the Global Regulatory Landscape

October 20, 2021
With medical device regulations tightening around the world, especially in Europe, it's important to assess the changes unfolding across the global regulatory landscape in... Read More
Regulatory Submission

Quality Insights from a 40+ Year Veteran of the Medical Device Industry

October 13, 2021
In this episode of the Global Medical Device Podcast, Jon Speer talks to Herschel “Buzz” Peddicord, founder and CEO of InControl Medical, which designs and... Read More
Product Development

When to Throw the Least Burdensome Flag on FDA

October 6, 2021
What if you submit your 510(k), IDE, or other submission type to FDA only to get an additional information request (AI request)? What do you do for requests that seem overly... Read More

Experience the Guru Edge

Our industry expertise extends beyond our software. Explore our other resources that are helping leading MedTech companies reach success.

Academy

Accelerate your learning and proficiency - both in Greenlight Guru solutions and industry best practices. You’ll be equipped to build key competencies for your teams.

Elevate Your Education
Community

You're not alone. We created a network of peers to connect with and learn from. At any stage of the product development lifecycle, become part of our community to accelerate your path to excellence.

Find Your Community
Partner Ecosystem

We have over 200 strategic partnerships with leading consultants in quality, regulatory, testing, design, and clinical.

Become a Partner
Resources

Do you have a unique problem that needs solving? Or maybe you’re just looking to elevate your expertise. If you're a MedTech professional looking to improve the quality of life for your patients, we have the right resources for you.

Explore Our Content Hub