Organizers
Partner: Lucendra | Medtech Consulting
Training Objective
- Get an overview of the regulatory landscape and regulatory stakeholders in MedTech
- Understand the major principles, concepts and processes
- Learn to sequence the necessary steps and build awareness of possible pitfalls when bringing a MedTech product to the market
- Know where and how to find required information
Target Audience
- Researchers in the field of translational medicine
- Employees from spin-offs, start-ups and SMEs, who intend to bring a product to the market
- Employees from companies interested in getting an overview on regulatory affairs
- Investors in medical devices who would like to understand risks and opportunities regarding the evolving regulatory framework in EU and US
Prerequisites
- Affinity to or involvement in MedTech or Life Sciences
- Basic understanding of good practices in product development and innovation
- Technical / scientific background or commercial background linked to Life Sciences products
The ticket fee includes lunch and coffee breaks.