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Greenlight Guru QMS

More than a Quality Management System: Tools for the entire MedTech Lifecycle.

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Featured Capabilities:

Document Management Product Development Design Control Risk Solutions Training Management CAPA Management

Experience the #1 QMS software for medical device companies first-hand. Click through an interactive demo.

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SMART-TRIAL by
Greenlight Guru

Data gathering and management designed for MedTech clinical trials and operations.

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Featured Capabilities:

Electronic Case Report Forms (eCRF) Electronic Patient Reported Outcomes (ePRO) Ad-Hoc Data Collection (Cases) Post-Market Surveys

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Greenlight Guru Academy

Learn valuable, career-boosting skills for the Medical Device industry. Get access to hundreds of free resources as well as subscription-based courses and certifications.

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Discover the new trends, outlooks, challenges, and opportunities in the MedTech industry in 2023.

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FREE ON-DEMAND VIRTUAL SUMMIT:
February 21-25, 2022

2022 State of Medical Device True Quality Summit Series

Greenlight Guru's annual State of Medical Device Product Development and Quality Management Report is coming to help you understand the strategies, tactics, and technologies used today to accelerate product development, ensure compliance, and promote quality.

Get the first look into the thoughts, findings, and data of original research from 500+ medical device professionals at this upcoming True Quality Summit Series.

Join us for just one hour a day to dig into the most compelling stats, biggest surprises, and must-know takeaways that will help you navigate uncertainty and maintain a competitive advantage this year.

Through engaging panel discussions and a deep dive into the report findings, you’ll discover what high-performing companies do differently and gain actionable insights to take your organization to the next level.

Sessions

Behind the Stats: 2022 Medical Device Product Development & Quality Management Benchmark Survey | Etienne Nichols

Balancing Innovation & Regulation: Navigating Design Development While Keeping Quality and Regulatory in Mind | Damini Agarwal, Shepard Bentley, Taylor Brown, Gaurav Manchanda, Jennifer Palinchik and Savanah Sitton

Quality Spotlight: Trials & Triumphs of Complaint Handling | Murtuza Bohari, Anne Holland, Joanne Lebrun and Wade Schroeder

The Path to Commercialization is No Easy Feat: Critical Milestones and Challenges | Adam Cargill, Rob MacCuspie, Sissi Miao, Tom Rish and Maxime Rochon

The Ins and Outs of Supplier Management | Mike Burgan, Shawn Findlater, Greg Lyons and Gaia Maurer

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Specifically, this summit series will cover:
  • What key issues are affecting the industry, including the 2022 revenue outlook, and quality management priorities and preparedness
  • What strategies, tactics, and technologies today’s medical device professionals are using to accelerate product development, ensure compliance, and promote quality
  • What are the biggest challenging about the runup to commercialization and what gaps are there in preparation
  • What high performing companies do differently (and how you can do the same at your organization)
  • What you can do to manage supply-chain risk
  • How to shift compliance-minded organizations to a True Quality mindset
  • What critical hurdles and headwinds you can expect to face post-commercialization (and how to conquer them)
Who should attend? 
  • Medical Device Executives & Leadership Teams
  • Quality Professionals and Management
  • Regulatory Affairs Professionals and Management
  • Clinical Affairs Professionals and Management
  • R&D Engineers and Management
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