ASQ Boulder 2025-Mar-27 Section Web Meeting

When:  Mar 27, 2025 from 11:45 AM to 01:30 PM (MT)
Associated with  Boulder Section

Topic: Is It Time to Redefine Quality
Cost: Free
Note: Thursday 11:45 am to 1:30 pm US-MT meeting
RSVP on Boulder Section’s meeting "Meetup Link"
https://www.meetup.com/boulder-quality-meetup/events/305218370/
RSVP note: Please provide your Name and Hometown. Same for any guests
11:45 am Web Conference Start: Networking, Welcome and Section Business
12:00 pm (Noon) Presentation

  • Speaker: Danny Even-Chen https://www.linkedin.com/in/dannyevenchen/
  • Topic: Is It Time to Redefine Quality
  • Presentation Slides and Video posted after meeting
  • Abstract:
    • As quality remains a cornerstone of brand trust, customer loyalty, and financial performance,
    • it is crucial for organizations to reassess Quality definition and implications via recent Technological, Global and Consumers paradigm shifts.
    • Quality needs a Multi-Dimensional adaptive and dynamic model that the interconnected dimension of Product, Service, Solution, Knowledge and Experience.
    • This changes "Quality" to be the integrated value created through multi-faceted delivery that meets stakeholders’ expectations by leveraging emerging technologies.
    • Learn how the Dynamic Quality Intelligence Model (DQIM) structured approach
    • Analyses current customers satisfaction levels as perceived by the relevant stakeholders on each quality dimension using emerging technologies.
    • This approach includes the following PDCA like phases:
      • Analysis
      • Enablers Transformation and Execution
      • Monitoring and Learning
      • Closed Loop Continuous Improvement
    • Contact Danny Even-Chen to learn, validate or improve DQIM via
  • Bio: Danny Even-Chen
    • Passion to drive innovative management and processes that result in best in class Medical Devices Safety, Quality, Reliability and Usability based on 25+ years experience.
    • Global Quality Systems management establishment for Medical Devices. Software as Medical Devices which comply with ISO 13485, QSR 820, EN 62304 , MDSAP and EU MDR.
    • Practices and training of Quality Engineering, Design for Safety (ISO 14971), Reliability, and SQA.
    • Global approbation of Medical Devices: 510(k), PAL, CFDA and EU MDR.
    • External audits by N.B. and FDA inspections.
    • Lead Q&R Due Diligence aspects for M&A followed by large scale integrations and change management.
    • Lead quality and regulatory of digital Informatics healthcare business.
    • Lecturer on Medical Devices Global Q&R challenges 
  • References:

1:15 pm After Presentation Networking
1:30 pm Web Conference End: meeting over
Place: Web Conference Webex


Meeting also posted on ASQ Boulder Meetup's 27 Mar 2025 meeting

Location

Online Instructions:
Url: http://asq.webex.com/asq/j.php?MTID=me0f8bd7d4bdb26218ac4d2ebd9dfc45c
Login: Place: Web Conference Webex Meeting link: https://asq.webex.com/asq/j.php?MTID=me0f8bd7d4bdb26218ac4d2ebd9dfc45c Meeting number: 2558 438 8282 Password: xJTwWygq524