Key Themes
Recognize how public policy impacts the medical device industry in terms of leadership and competitiveness in the world
Identify the opportunities and challenges in various regulatory markets, alongside an analysis on potential modifications to 510k policy
Incorporate performance, safety, business economics, risk management, and regulatory requirements as a basis for device design
Understand the impact of the IMDRF and increased harmonization in the Medical Device Industry
Leverage digital manufacturing to accelerate time to market while reducing risk
Create a successful partnership with suppliers and contract manufacturers
Apply ‘Design Thinking’ as a driver for medical device development
Lower the cost of product R&D while improving speed to market
Utilize your post-market surveillance system to feed your risk management and product lifecycles
Reduce up-front investment and market risk through effective and frequent prototyping early in the development cycle
Ensure that the design of the medical device can be correctly translated into production specifications
Develop and sustain the gains of a quality culture and adopt proven change management techniques
Venue
The Westin Lombard Yorktown Center
70 Yorktown Center, Lombard, IL, 60148
+1 (630) 719-8000
Get in Touch
555 Richmond Street West, Suite 1106
P.O. Box 119
Toronto, ON, Canada, M5V 3B1
