Exhaustive Extractions

At iuvo, we work hard to stay on the cutting edge of new developments in testing and regulatory changes affecting the medical device and pharmaceutical industries. We will share these updates regularly here in our blog - Exhaustive Extractions.

Join us for our Webinar on Biocompatibility and the EU MDR

iuvo will be teaming up with R&Q for a webinar on Biocompatibility: EU MDR and the Changing Regulatory Landscape.  The webinar is March 26, 2019, from 1-2pm ET. The slides, webinar recording, and Q&A will be made available to registrants after the webinar.

 

The session will dive into the increased specificity of the EU MDR from a biocompatibility perspective and how the revised 10993-1 fits into the requirements. We'll share our experiences from the viewpoint of testing laboratory experts and regulatory consultants with biocompatibility experience from both science and regulatory affairs backgrounds.

Our combined expertise has you covered!

The goal of the webinar is to help you understand the changing regulatory landscape in light of EU MDR, what that means for biocompatibility, and how to ensure your products have adequate evidence.

To register, click here or on the image below to go to the registration page.  

Webinar 3 26 19

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