The core activity of Easy Medical Device GmbH is to provide services in the field of medical devices, particularly in the areas of quality assurance and regulatory affairs. This includes, among other things: Consulting for medical device companies, Support in complying with regulatory requirements such as MDR, FDA registration and MDSAP certification, Conducting supplier audits and mock inspections, Creating and updating technical documentation, clinical evaluations and post-marketing surveillance systems, Selecting and supporting the implementation of UDI providers and European Authorized Representatives, Coaching for the career development of medical device professionals. The company supports medical device companies in fulfilling their regulatory obligations and helps them bring their products to market.