You are a start-up company or new to the medical technology market? Finding yourself confronted with many new legal requirements?
For example, the EU-Medical Devices Regulation(MDR) requires documented processes or you need certification according to DIN EN ISO 13485.
Downloading the regulation or buying the standard and understanding the requirements is one thing – but finding a way to implement these requirements is another.
BEO BERLIN BEO BERLIN helps by addressing the issue together with our clients. You explain your company to us and we give you ideas and tools to implement the legal/standard requirements in such a way that not only the requirements are met, but added value is created for your company.
