Learn what is required to go from research to approval of a new medical technology.
Medical devices and new diagnosis technologies are playing an increasing role in medical care. Progress in engineering and life sciences, specifically genomics, are opening the door for the development of new tools for the prevention, monitoring, diagnosis, treatment and even aftercare of patients. For those technologies to become available they need to undergo an exacting regulatory approval process that requires up-to-date knowledge of the latest regulations and research. Explore the programs we offer that will help you understand how to design, develop and deliver medical devices and diagnostics in this growing industry.
This 3-day workshop will expand your knowledge of the latest innovations within the biomarkers field.
Learn the requirements for moving an IVD product from concept to regulatory approval and market launch
Hear about upcoming events and courses