February 20 2020


1MED boasts a multi-disciplinary team with expertise in design, engineering and certification of medical devices, combination products (drug-device) and in vitro diagnostics.
Given the wide knowledge and experience, our Regulatory Affairs Managers and Regulatory Specialists are also qualified by some of the most important Notified Bodies to support medtech companies in training activities within the Quality, Clinical and Regulatory field, with focus on the requirements highlighted in the new European Medical Device Regulation (MDR) 2017/745.

We can support your company with tailor made on-site and off-site training programs that focus on your company’s specific needs on a wide range of Regulatory, Clinical and Quality subjects.

We are at your disposal to get into details on your company’s training needs, so please do not hesitate contacting us for more details.