FREE ON-DEMAND VIRTUAL SUMMIT:
January 23-27, 2023

2023 State of Medical Device True Quality Summit Series

Greenlight Guru's annual 2023 MedTech Industry Benchmark Report is coming to help you understand the strategies, tactics, and technologies used today to accelerate product development, ensure compliance, and promote quality.

Get a first look into trends, outlooks, statistics, and opportunities in the medical device industry from data gathered from 600+ medical device professionals at this upcoming True Quality Summit Series.

Sessions

Behind the Stats: Expectations vs. Reality of Bringing a Device to Market | Etienne Nichols and Radhika Pandya

Leveraging Modern Software Technologies: MedTech’s Best Kept Secret | Damini Agarwal, Som Pathak, Michael Roberts and Maxime Rochon

The ROI of Shifting Mindset From Compliance to Quality | Edwin Chung, Aaron Gifford, Daniel Powell and Jeff Schwegman

How Electronic Data Capture Is Transforming the MedTech Industry | Jon Bergsteinsson, Autumn Dawn Lang PhD, RAC and Rianne Tooten

The Compliance Concern: Challenges and Roadblocks for Ensuring Compliance in 2023 | Carlos Almeida, Amanda Feddersen, Weronika Michaluk and David Shanes

Watch the Summit Series

Q1 2023 VS Graphic-1
Specifically, this summit series will cover:
  • What key issues are affecting the industry, including the 2023 revenue outlook, 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
  • How software technologies that MedTech is using can be the value multiplier for their business
  • What tools the MedTech industry is using to manage critical processes for QMS and EDC systems
  • 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
Register Now  

A few of the experts...

Etienne-Nichols-white-bkgnd
Etienne Nichols

Medical Device Guru & Community Manager,
Greenlight Guru

Radhika headshot
Radhika Pandya

Product Marketing Specialist,
Greenlight Guru

Damini Agarwal
Damini Agarwal

Director of Product Development,
Infinite Biomedical Technologies, LLC.

Som Pathak
Som Pathak

CEO,
NSV

Michael Roberts
Michael Roberts

Vice President, Sales & Marketing,
SPK and Associates

Maxime Rochon
Maxime Rochon

Director, Quality Assurance and Clinical Affairs,
Puzzle Medical Devices

Edwin Chung
Edwin Chung

Director of Engineering,
SPK and Associates

Aaron headshot
Aaron Gifford

Principal Engineer,
Nectar

Daniel Powell
Daniel Powell

CEO,
Spark Biomedical

Jeff Schwegman
Jeff Schwegman

Vice President of Engineering,
Recovery Force

Jon headshot
Jon Bergsteinsson

Co-founder of SMART-TRIAL by Greenlight Guru,
Greenlight Guru

Autumn headshot
Autumn Dawn Lang PhD, RAC

Director Clinical Affairs,
VeriSkin Inc.

Rianne headshot
Rianne Tooten

Founder,
Rianne Tooten

Carlos Almeida
Carlos Almeida

Vice President of Engineering,
SPK and Associates

Weronika Michaluk
Weronika Michaluk

Digital Health Principal,
HTD

David Shanes
David Shanes

Vice President of Regulatory Affairs,
Fullpower Technologies Inc.

Amanda headshot
Amanda Feddersen

Quality Assurance Manager,
Monitored Therapeutics Inc.

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