29. September 2020
Workshop: Introduction to product developement and regulatory affairs
Do you want to understand how product development and regulatory affairs (MDR/IVDR) needs to work together to successfully bring products to market?
Then our workshop with Nila-Pia Rähle is right to you! She provides an overview of the regulatory landscape for medical devices in Europe (MDR/IVDR) and touch upon different aspects for USA. You will get a good understanding of the product development process, as well as the requirements regarding technical documentation.
Register now – space is limited!
October 15, 1pm – 5 pm
In the offices of Effectum Medical, 4th floor, Solothurnerstrasse 235, 4600 Olten (Usego Areal). The valid protection provision for COVID 19 are implemented.
Fee for start ups 200 CHF (alternatively via Innosuisse voucher), all others 300 CHF . Number of participants is limited to four.
For more information:
EM-Workshop "Introduction to Product Development and Regulatory Affairs" (45 downloads)
or just register by sending an e-mail to email@example.com.
Looking forward to welcome you.
Your Effectum Medical Team