What is the difference between claiming equivalence under EU MDR compared to MDD?
What are the key requirements for demonstrating equivalence?
What can improve the process of demonstrating equivalence under the EU MDR?
We answers your questions and more…
Manufacturers can circumvent the time and expense of conducting clinical studies to satisfy the safety and performance requirements as outlined in the clinical evaluation by claiming equivalence with another device to get CE certification under the MDR.
We provide services globally, so reach out via this contact page and we will reach out to you, within 12 hours to discuss how we can help.
