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About the Author

Nick Tippmann is the Chief Marketing Officer for Greenlight Guru, a MedTech Lifecycle Excellence Platform (MLE) that provides an industry-specific solution to help medical technology innovators around the world use quality as an accelerator to move beyond baseline compliance and achieve True Quality. Tippmann is 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.

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... Read More
FDA Regulations

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... Read More
FDA Regulations

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
FDA Regulations

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... Read More
Product Development

Case Study: How a Partnership with Greenlight Guru is Making This Dental Device Manufacturer Smile

September 28, 2021
{% video_player "embed_player" overrideable=False, type='scriptV4', hide_playlist=True, viral_sharing=False, embed_button=False, autoplay=False, hidden_controls=False,... Read More
FDA Regulations

Case Study: How The Partner Ecosystem Has Been Key To Market Success For Spark Biomedical

September 24, 2021
“Having partners with common values is just as important as the product or services themselves.” Daniel Powell, CEO Read More
Medical Device Industry

Greenlight Guru Opens New Global Headquarters in Downtown Indianapolis

September 23, 2021
Fast-growing software company to host grand opening event to celebrate company’s investment in growth in Indianapolis tech community Read More
FDA Regulations

Past, Present, Future State (and World) of Quality in the Medical Device Industry

September 22, 2021
Quality is a concept that is often overcomplicated in the medical device industry. With complexity comes mistakes, which is why it's so important for manufacturers to ... Read More
Quality Management System (QMS)

True Quality: Greenlight Guru consistently ranked the #1 QMS by users for three years in a row

September 16, 2021
Greenlight Guru is proud to announce that for three years straight, we have been named the leader in G2’s Quality Management (QMS) category, following the recent release of... Read More

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