Regulatory is part of our DNA
Regulations are a complex matter. From PPER (Personal Protective Equipment Regulation) and MDR to IVDR (In Vitro Diagnostic Medical Device Regulation) and BPR (Biocidal Products Regulation) , and beyond. The first questions from customers are often: “Which products does it cover?” “Are these regulations relevant for me?” “What’s the deadline?”
No matter what your question, product, or regulation, at HARTMANN we can tell our customers, “We’ve got this.” Because we have a clear action plan. Our regulations team continuously invests in research and exchange with collaborators like TÜV SÜD and industry organizations to ensure we are always a reliable partner to our customers.
HARTMANN products: regulation ready, and ready to deliver
We’ve got this.
As your reliable partner, our strategy is clear: we take care of regulations so you can take care of your patients. Ensuring your safety and the safety of your patients is our number one priority.
We’re a first mover.
We set our regulation action plan into motion years ago, meaning that today HARTMANN lies well ahead of the competition in terms of regulation compliant products.
We partner with the experts.
For us to have your back, we need the right partners. HARTMANN works directly with its key Notified Body TÜV SÜD – so we benefit from timely certifications, and you can continue to rely on delivery of safe products.
Security of supply is our priority. In the event of product range adjustments, we provide detailed information and, where possible, offer adequate substitute products.
Looking for regulation compliant products?
Look no further. If your supplier can’t ensure delivery of, for example, MDR compliant devices, contact HARTMANN. Because we can deliver. We’ll find the best regulation-ready products for your needs.