Informatica Experts offers specialist consultancy, training and resource in delivering and implementing compliance of the new EU medical device (e.g. EUMDR 2017/745) regulations across your data systems and processes.

Informatica Experts appreciates that the need to initiate these changes is immediate and overwhelming. We are able to source and provide the experts, teams and resources required to ensure your company is able to meet the new regulations. We can provide the workforce that will be able to manage the additional hours, understand the regulations and facilitate the implementation. We can also train your existing staff, leaving you with full peace of mind that you will be compliant with the new regulations.