LSX Medtech Devices CEO Forum

2021 session details

Agenda | Attendees | Hosts | Book

Open to CEO, Founder, Co-Founder, President, Chairman or c-suite executives (CFO, CBO, CCO, CSO, CMO) of US-based Medtech device companies.

Free to attend, pre-registration only, Chatham House Rule forum hosted on Zoom where all participants are active discussants. 

  • Benchmark yourself against your peers
  • Uncover key factors of success
  • Share war stories and common challenges
  • Engage in peer-to-peer discussion
  • Make meaningful connections
  • Find new ways to help your business thrive


Agenda (All times in EDT)

13:00 Welcome

Introduction from LSX to the forum, introductions from all participants and sharing of pre event benchmarking survey results


13:05 Client Alliance Perspective Case Study with Q&A: How to Supercharge Your New Product Development Introduction Processes: Design Control, Risk Management & QMS Best Practice

  • How to streamline the management of device requirements, risk, design reviews, and documentation.
  • How to easily demonstrate closed-loop traceability throughout your quality, design, and risk processes.
  • How to automate quality processes with the right guardrails in place to assure compliance and keep your team audit ready
  • How an electronic quality management system can lay the foundation to meet your needs today and scale with you tomorrow

Jon Speer, Founder, Greenlight Guru
Ryan Shelton, CEO & Co-Founder, Photonicare

Jon Speer, Founder, Greenlight Guru 300x    Ryan Shelton, CEO & Co-Founder, Photonicare


13:25 Executive Led Case Study: Navigating Market Access Challenges Across Different Clinical Areas

  • Cost adoption for pivotal trials
  • Capital Preservation: How to make progress
  • Knowing your market, what to implement and when
  • Capital Preservation: How to make progress

Chuck Carignan, CEO, Sonivie

Chuck Carignan, CEO, Sonivie


13:35 Interactive discussion and Q&A


13:50 Breakthrough Designation and MCIT Delay

A conversation on the implications and considerations for innovators

John Doucet, former FDA Policy Lead of the Breakthrough Device Program, MCRA
Tonya Dowd, Vice President, Reimbursement, Health Economics and Market Access, MCRA

John Doucet, Senior Director Neurology Regulatory Affairs, MCRA 300x    Tonya Dowd, MPH, Vice President, Reimbursement, Health Economics & Market Access, MCRA 300x


14:10 Executive Led Case Study: Double Down Or Trade Up: The Critical Impact Of Digital Within Devices

  • Identifying your market exposure and adapting to current conditions
  • Adapting to the change in landscape following the rise of pharmacy and urgent patient care
  • Implementing strategic investment plans

Giles Hamilton, CEO, ODx Innovations

Giles Hamilton, CEO, ODx Innovations


14:40 General Discussion (suggested topics to include but not limited to)

  • The smoothest route to successful clinical progression
  • Overcoming barriers to market and regulatory approval
  • Defining the best deals and partnerships to strategically move your business forward


15:00 Close Medtech Devices CEO Forum


Join:

    Advanced Scanners    Agile Devices    Biorez  Sonivie   
    Ponce De Leon Health    TYBR Heatlh    Blumio  Snoasis Medical   
    Neurescue    PhotoniCare    Novian Health Naiad Lab    
    Scanbo Technologies    Cognoptix        Bresotec Inc     Encora Therapeutics    
         Zilia Inc          Rhinostics        Sonavex     TomoWave Laboratories    
     Windgap Medical     Zeto    Alertgy     Proactive Diagnostics    
     Rapid Nexus    Digital Diagnostics    Puzzle Medical Devices    ODx Innovations 300x    


Co-hosts:

    Greenlight Guru    MCRA 300x    

 

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