Medical Device Software Development: How to Build your EU/US Strategy
Published on: May 11th, 2020
This webinar helps developers of e-health/m-health solutions to better understand the regulatory environment relevant to their digital technologies in Europe and in the US and how to best overcome these challenges to maximize the chances of a timely and successful market launch on these markets. This webinar outlines how e-health/m-health companies can implement strategic development plan for their products with the aim to minimize the risks and to avoid the introduction of extra delays for reaching the EU and US markets. Opportunities and cautions for placing on these markets such as innovative AI-based and other digital solutions will be shared.
Key topics include:
EU/US regulatory frameworks applicable to e-health/m-health technologies
e-health/m-health product development and evaluation under Medical Device scheme
Critical challenges for placing e-health/m-health solutions on the market in the EU and the US
SAMPLE OF THE WEBINAR
