Date: Wednesday 14 July, 4-5pm
Venue: Online
Register: Here
In this Gateway to Translation webinar, Ms Tara Fahy, Regulatory Affairs/Quality Consultant at Med-Di-Dia Ltd., Ireland (the Irish subsidiary of Global Regulatory Services Ltd.) will discuss how to establish medical device classification through regulatory pathways to achieve successful commercialisation. To register, please click here.
Date:
Wednesday, 14 July, 2021 - 16:00 to 17:00
