Strategic advice & planning

Executive management needs to be guided and directed by its compliance staff however the new EU Medical device regulations are complex and difficult in timing, implementation and in establishment.

We provide full consultancy support for the development and implementation of your market access strategy. We combine an understanding of the global Regulatory- and Quality Systems requirements having access to professional and experience consultants at all stages of global Medical Device Regulations.

MDRcare is able to support your compliance department/management with compliance experience, strategy, planning and understanding requirements on-site and off-site.