29. September 2020
Workshop: Introduction to product developement and regulatory affairs
Do you want to understand how product development and regulatory affairs (MDR/IVDR) need to work together to successfully bring products to market?
If the answer is a ‘yes’, this workshop by Nila-Pia Rähle is for you. The course will provide participants with an overview of the regulatory landscape for medical devices in Europe (MDR/IVDR) and will also touch upon different aspects for the US market. Participants 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" (147 downloads)
or just register by sending an e-mail to firstname.lastname@example.org.
Looking forward to welcome you.
Your Effectum Medical Team