Are you seeking insights into navigating the European regulatory landscape for medtech products? If the answer is YES, sign up now for the free Notified Body Increased Capacity (NoBoCap) program on MDR/IVDR implementation and resource and budget allocation, adapted for C-level management. The first and last sessions will be held in-person at Sensum, Kortrijksesteenweg 1026,Ghent, while the remainder will be virtual.
NoBoCap’s program kicks off on 17 May with a half-day in-person seminar on marketing medtech products in Europe’s highly regulated landscape.
9:30 – Reception with coffee
9:45 to 11:00 – Part I
11:00 to 11:15 – Coffee break
11:15 to 12:30 – Part II
12:30 – Sandwich lunch
The sessions continue weekly with one-hour webinars on the following topics:
- Investments need to bridge Europe’s “regulatory valley of death”
- Selecting a Notified Body for your medtech product
- Developing quality management NoBoCap systems and documentation
- Start-up case study on investing at the right time
The program culminates on 21 June with a half-day in-person seminar focused on exchanging experiences.
For more information about the NoBoCap program and to register, visit the NoBoCap website.
