MDR & Drug-Device Combination Products with Theresa Jeary

Medical Device made Easy Podcast · Apr 13, 2020

This episode will be really interesting for the pharmaceutical companies that are producing Drug-Device combination products as it explains the consequence of EU MDR Article 117 for their products.

For all projects that are ongoing, you need to consider the new requirements coming from EU MDR as this is amending the 2001/83/EC Medicinal Product Directive.

Theresa Jeary will be my guest during this episode, and her experience with Drug-Device products and as a former Notified Body assessor will help you understand what are the deliverables you should provide now.

We will also discuss the…