Greenlight Guru Takes Medical Device Quality & Regulatory Roadshow Global in 2020

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The second annual True Quality Roadshow to gather industry-leading professionals for expert insights and education on the changing regulatory landscape

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"Having recently compiled one of the most comprehensive studies of the medical device industry, we plan to drill down to the deeper issues facing our industry alongside some of the most brilliant minds within our industry."

Greenlight Guru, the only medical device quality management system (MD QMS), today announced the 2020 True Quality Roadshow, an eight-city, global gathering of medical device professionals and industry stakeholders.

The 2020 True Quality Roadshow will include a networking event and panel discussion where industry professionals will offer their personal experience and thoughts on the recently released State of Medical Device Product Development & Quality Management Report 2020, as well as a live recording of the Global Medical Device Podcast, the most downloaded podcast in the medical device industry. This year, the show has also expanded globally with a stop in Dublin, Ireland.

“In 2019, we launched the True Quality Roadshow on the heels of our partnership with the FDA to promote the benefits of their Case for Quality initiative. We brought together more than 400 medical device professionals in seven U.S. cities, and this year, we’re expecting many more with the addition of a stop in Dublin, Ireland,” said Jon Speer, Founder & VP of QA/RA at Greenlight Guru. “Having recently compiled one of the most comprehensive studies of the medical device industry, we plan to drill down to the deeper issues facing our industry alongside some of the most brilliant minds within our industry.”

Greenlight Guru’s State of Medical Device Product Development & Quality Management Report 2020 found that 81% of medical device companies are not using tools designed for the medical device industry within their quality management processes. Furthermore, 75% of medical device professionals said that they would not be prepared for an unannounced audit by the FDA or other Notified Body.

The True Quality Roadshow which will be hosted in leading medical device hubs across the world will evaluate the report as experts offer their personal insights on the findings. The first stop of the roadshow will be San Jose, California in February 2020.

  • San Jose, Calif. – February 6th
  • Houston, Texas – February 26th
  • New York City, N.Y. – March
  • Boston, Mass. – April
  • Dublin, Ireland – April 20th
  • Minneapolis, Minn. – May 21st
  • San Francisco, Calif. – June
  • Chicago, Ill. – July 16th

The True Quality Roadshow follows the announcement of the State of Medical Device Product Development & Quality Management Report 2020 and the fifth straight quarter Greenlight Guru was named a market leader according to G2 Crowd, the first and only vendor to be recognized as such in the category.

To learn more about attending the roadshow in a city near you and partnership opportunities, please visit https://www.greenlight.guru/events/true-quality-roadshow.

About Greenlight Guru
Greenlight Guru is the only quality management software platform designed specifically for medical devices companies. The platform helps companies bring safer products to market faster, simplifies FDA and ISO regulatory compliance and provides a single source of truth by connecting the management of all quality processes like CAPAs, risk, audits and more. Greenlight Guru’s platform is used by thousands of users across the globe to push beyond baseline compliance and achieve True Quality for their medical devices. For more information, visit http://www.greenlight.guru.

Media Contact
Kate Johnson
kate_johnson@blastmedia.com
(317) 806-1900 ext. 144

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Kate Johnson
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