We offer more than 20 years of practical experience in consultancy and device development in the field of medical devices.
Our customer portfolio ranges from new start-ups to established SMEs and multinational companies, for whom we have created and implemented projects successfully.
Due to our broad and network based knowledge we take responsibility for global product certifications and the successful implementation of quality management systems in accordance with ISO 13485 / 21CFR820 tailored to the company in question's needs.
Our many years of professional activity in product development of medical devices and their manufacturing processes ensures a value-adding support for our cutomer's operations as well.
Our close contact and collaboration with authorities, notified bodies and partner companies guarantee that our customers will pass regulatory obstacles with ease.
We would be happy to discuss several reference projects with you directly and look forward to talking to you soon!