Thursday, June 3, 10:00 am - 1:00 pm ET

Join our first MedTech Quality Community Meeting to connect with peers and strategy experts to learn and share best practices to modernize quality. You'll hear use cases from experts leading digital transformation, get a product roadmap update, engage in live Q&A, and have the opportunity to join roundtable discussions.
You'll walk away with actionable insights to enhance quality operations and processes that will help improve speed to market, product quality, and innovation.

Agenda (ET times):

10:00 am - 10:30 am Opening Keynote: The Case for Quality - Data Driven Modernization
10:30 am - 11:15 am Customer Panel: Drivers & Best Practices for Modernizing Quality
11:25 am - 12:25 pm Quality Product Roadmap
12:30 pm -  1:00 pm  Roundtables

If you are not able to attend the full event you can still register to attend a portion of the meeting.


Joseph Sapiente - Keynote

Associate Vice President, Case for Quality

Medical Device Innovation Consortium (MDIC)

Joe has 38 years of medical device experience in quality and regulatory compliance, product registration, continuous improvement, and new product development and innovation. He has held executive roles with Hologic, Medtronic, Covidien, Tyco HealthCare, and US Surgical.

Alon Ben Jacob

Director, Quality Acquisition & Divestiture

Johnson & Johnson

With 18+ years of industry experience as a Quality & Compliance executive leading teams for several global leading technology companies, Alon brings multi-disciplinary quality expertise that enables him to act as an end-to-end quality leader at J&J.

Tracy McKinney

Head, Quality Information Systems


Tracy partners with global, cross-functional teams to facilitate the implementation of quality systems strategy focusing on compliance and process efficiencies.

Mark Ramser

Senior Global Director, Quality Assurance


Mark has global responsibility for all quality related activities at Epredia, and a professional history of harmonizing quality management systems globally to meet compliance requirements.

Kareem Elwakil



Kareem specializes in transformation across the medical device value chain, and advises clients on a range of topics, including quality strategy, systems, and operations.

Register Now

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