Greenlight Guru
Greenlight Guru is the #1 provider of modern cloud-based solutions for the MedTech industry, helping companies bring life-changing products to market faster, more efficiently, and with less risk.
Greenlight Guru’s MedTech Suite provides quality management, product development, and clinical data management solutions, along with high-quality training and education required to keep up with the rapidly changing industry regulations.
Trusted by over 1,100 medical device companies across the globe, Greenlight Guru has been named by G2 as the #1 Medical QMS Software and by the Inc Magazine as a Best Place to Work. For more information, visit www.greenlight.guru.
San Jose True Quality Roadshow Panel Discussion
What to look for in a Medical Device industry conference
The Most Important Thing In Medtech
The Reasons Medical Device Companies Fail
The Least Burdensom Method of QMS
Medical Device Development Best and Worst Practices
Getting your Medical Device Management Back On Track
Changes in Medical Device Regulatory Agencies
Amsterdam | LIVE Recording of Global medical Device podcast - 2023 Roadshow
Orange County, CA | LIVE Recording of the Global Medical Device Podcast
Orange County, CA | 2023 True Quality Roadshow
Minneapolis, MN | LIVE Recording of the Medical Device podcast
Minneapolis, MN | 2023 True Quality Roadshow
Minneapolis, MN | LIVE Medical Device Podcast - 2023 Roadshow
San Jose, CA | 2023 True Quality Roadshow
Boston, MA | LIVE Recording of Global medical Device podcast - 2023 Roadshow
Boston, MA | 2023 True Quality Roadshow
San Jose, CA | LIVE Recordings of Global Medical Device Podcast - 2023 Roadshow
Houston, TX | LIVE Recording of the Global Medical Device Podcast
Houston, TX | 2023 True Quality Roadshow
2021 State of Medical Device Quality Management & Product Development Report Findings
3 Powerful Ways to Revolutionize your Approach to Closed-Loop Quality System Traceability
3 Ways Medical Device Companies are Leveraging QMS Software to Foster Innovation and Collaboration
How to Integrate Risk Management throughout the Lifecycle of a Medical Device in the Coming Decade
Panel Discussion - Houston
#408: What MedTech Startups Miss: Design Mistakes, Risk Testing & the Myth of the Quick Exit
#407: Cybersecurity in MedTech: FDA Compliance, Patient Safety & the Hidden Risks You’re Missing
#406: Over the Counter (OTC) vs. Prescription (RX) Medical Devices, Pt. 2
#405: Over the Counter (OTC) vs. Prescription (RX) Medical Devices, Pt. 1
#404: MedTech 101: What You Need to Know About the Medical Device Industry