At dsm-firmenich Biomedical we take our responsibility to patients, partners, and society seriously.
We comply with all applicable regulatory requirements and maintain FDA Material Master Files for many of our products.
This is all based on our comprehensive understanding of how the human body reacts to biomaterials following implantation – which in turn enables us to design biomaterials that are fully compatible with the body’s physiology. For our partners, the result is innovative medical devices that sustain, restore, repair – and ultimately bring progress to life for patients everywhere.
Contact us to explore how we can accelerate your product development.
We hold the following certifications for dsm-firmenich Biomedical operations worldwide.
MDSAP 669973 Certified
ISO 13485:2016 Certified
FDA Registered
ISO 13485:2016 Certified
ISO 13485:2016 Certified