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" (85 downloads)

or just register by sending an e-mail to workshops@effectummedical.com.

 

Looking forward to welcome you.

Your Effectum Medical Team