Compliance with the Medical Device Regulation (EU) 2017/745 (MDR) presents many new challenges to Medical Device manufacturers. Our in-depth MDR training is designed to help you and your team prepare for these challenges and transition smoothly to the MDR.
This course focuses on what is required to bring your Medical Device to market under Medical Device Regulation (EU) 2017/745 (MDR)
The course is intended for individuals that work for a Medical Device manufacturer or CMO who's responsibilities require them to have an understanding of Medical Device Regulation (EU) 2017/745 and the differences/issues from the current MDD. In particular Quality Management, Quality Assurance, Regulatory Affairs, Design and Development, Clinical Affairs Specialists, Authorized Representatives, Economic Operators, including importers and distributors.
This course focuses on what is required to bring your Medical Device to market under Medical Device Regulation (EU) 2017/745 (MDR)
The course is intended for individuals that work for a Medical Device manufacturer or CMO who's responsibilities require them to have an understanding of Medical Device Regulation (EU) 2017/745 and the differences/issues from the current MDD. In particular Quality Management, Quality Assurance, Regulatory Affairs, Design and Development, Clinical Affairs Specialists, Authorized Representatives, Economic Operators, including importers and distributors.
