The core activity of MedTechXperts GmbH is to advise and support companies in the medical technology industry in complying with regulatory requirements and quality standards, particularly with regard to the approval and market access of medical devices. This includes, among other things: * Regulatory Affairs: Consulting and support in complying with regulatory requirements such as the EU Medical Device Regulation (MDR) and FDA regulations * Quality Management: Consulting and support in implementing quality management systems and complying with quality standards such as ISO 14971 * Engineering and Innovation: Consulting and support in developing medical devices and implementing innovative solutions * Clinical Evaluations and Investigations: Consulting and support in conducting clinical studies and creating clinical evaluation reports * Project Management: Consulting and support in planning and executing projects in the field of medical technology The company supports small and medium-sized enterprises as well as start-ups in complying with regulatory requirements and rapidly bringing their products to market.