In this 7th edition of the Conference you will have the opportunity to gain a better understanding on the new European regulations on medical devices. Additional regulations (implementing acts) of the Medical Device Regulation and new guidance are issued frequently adding to the complexity. It is important to keep up-to-date with the fast evolving compliance scene. This event addresses to all those involved in the medical device field worldwide, such as Medical Device Companies, R&D and QA personnel, CEOs / CROs / CRAs, Regulatory Affairs Specialists, Research facility managers, Pharmaceutical Company representatives and Start-Up Companies. In conjunction with EAAR (European Association of Authorized Representatives), our excellent panel of experienced professionals in this field will once again ensure a conference of noteworthy quality.