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