American Medical Device Summit

The American Medical Device Summit is dedicated to medtech design innovation, regulatory harmonization, and more.

Key Topics

• Post-market surveillance system to feed risk management and product life cycles
• The impact of public policy on the medical device industry in terms of global market expansion and competitiveness
• Effective collaboration through third party inventory ownership and Asset-as-a-Service solutions
• The opportunities and challenges in various regulatory markets, alongside an analysis on potential modifications to 510k policy
• Reducing up-front investment and market risk through effective and frequent prototyping early in the development cycle
• Leveraging existing commercial terms with suppliers while improving balance sheet efficiency
• Design Thinking as a driver for medical device development
• Performance, safety, business economics, risk management, and regulatory requirements as a basis for device design
• The impact EU MDR and increased harmonization in the medical device industry
• Translating design of the medical device into production specifications
• The gains of a quality culture and proven change management techniques
• The next generation of medical devices and value-based health care

Who should Attend

Medical device leaders with job titles such as:

• VPs
• CEOs
• Directors in the medical device industry with responsibilities in supply chain, manufacturing, operations, technology, regulatory affairs and quality assurance