Join this free webinar to learn how to navigate the regulatory roadmap for medical combination products.
In this webinar you will learn:
- Why you need market approval
- How do you determine which regulations are applicable to you as a manufacturer
- What technical documentation you need
- How combination products are regulated by the FDA.
At the end of this webinar, you know where to start with building the file for your drug device combination product.
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About BioMan4R2
The BioMan4R2 project within the European SMP COSME program offers financial support and networking for small and medium-sized companies in the biological products and medical technology manufacturing sectors that want to increase their resilience, sustainability and competitiveness. The partner regions in Europe for this project, together with LifetecZONe are Business Turku Oy Ab (FI), BioRegio STERN (DE), Medicen Paris Region (FR), GAPR the Upper Silesian Accelerator for Commercial Enterprises Ltd (PL), Council of European Bioregions and Biocat (ES).