FREE ON DEMAND WEBINAR

Manufacturing of medical devices, design transfer and heading into the unknown

While the MedTech world buzzes with talk of EU MDR and FDA submissions, the equally critical phase of manufacturing is often left in the shadows. Join Adnan Ashfaq—Founder-Director at Simplimedica Ltd and a rare blend of Manufacturing Engineer and Regulatory Consultant—as he sheds light on what really happens after Design Transfer.

Specifically, this webinar will cover:

  • Why production is a hotbed for non-conformances—and how to prepare for it
  • Time-tested principles from manufacturing legends like Deming, Juran, and Shigeo Shingo
  • Japanese techniques such as SMED, Kanban, OEE, and Kaizen in the context of MedTech
  • Real stories from the floor: AI, machine vision systems, and the tension between innovation and job security
  • What today’s startups need to know as they head into the “unknown” of scaling production

Whether you're a quality leader, regulatory consultant, or MedTech founder, this is your chance to rethink Design Transfer not as an endpoint—but the beginning of your next biggest challenge. The webinar will conclude with a live Q&A session.

Watch the on demand webinar

2025 | GG Webinar Simplimedica Medical Device Design Transfer - 4-24-25-1
Who should attend?
  • Quality Professionals and Management
  • Regulatory Affairs Professionals & Management
  • Medical Device Executives
  • Product Development Engineers and Management
Register Now  

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