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!
Time:
October 15, 1pm – 5 pm
Location:
In the offices of Effectum Medical, 4th floor, Solothurnerstrasse 235, 4600 Olten (Usego Areal). The valid protection provision for COVID 19 are implemented.
Price:
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"
or just register by sending an e-mail to workshops@effectummedical.com.
Looking forward to welcome you.
Your Effectum Medical Team
