Sounds complicated? And what if my product is both?
Do not worry! In this webinar we will explain:

1.Why you need market approval
We will start by explaining the basic structure including the differences and similarities between CE marking and marketing authorization.

2.How do you determine which regulations are applicable to you as a manufacturer
Your device can never be a medical device AND a medicinal product. You need to choose which set of rules is applicable for your product. We will explain how to determine this.

3.What technical documentation you need
Once you have determined which rules are applicable, the rules prescribe which documents you need. We will give a short overview of the documentation required for medical devices and medicinal products.

4. Voyage to the new world
With an initial grasp of regulatory requirements in the EU and an idea of how to get started, we glimpse across the Atlantic to discuss how combination products are regulated by the FDA. We will explain entities involved and describe how you can approach them, where precedent can be found and what guidance is available to you.
At the end of this webinar, you know where to start with building the file for your drug device combination product.
This training is brought to you by the Dutch companies Holland Innovative, experts in medical device development, and Interdos, experts in medicinal product development and registration, and the German company novioneon CRO GmbH.

More information about the BioMan4R2 project you find on the project page.