✿(a) a diploma, certificate or other evidence of formal qualification, awarded on completion of a university degree or of a course of study recognized as equivalent by the Member State concerned, in law, medicine, pharmacy,
engineering or another relevant scientific discipline, and at least one year of professional experience in regulatory affairs or in quality management systems relating to medical devices; ✿(b) four years of professional
experience in regulatory affairs or in quality management systems relating to medical devices.
.png "qadvis_web-300x138_180925")
.png "qadvis_web-300x138_180925")
