Are you ready for change?
The medical device regulation (MDR) has now entered into force and will apply from May 2021. Since this is a regulation and not a directive it will be part of the local regulation in all member states. Transitioning to MDR will be challenging. If you have not initiated work yet, or are still in the early stages, we can help you to take a major step forward.
At PlantVision we have extensive experience working with all areas of regulatory compliance. We offer a range of flexible MDR support services including workshops, seminars, gap analysis, transition planning, continuous support and training.
Combined SEMINAR & WORKSHOP
Get things moving in the right direction. Arrange a free TWO HOUR seminar & workshop with our MDR specialists.
We will come to your company and introduce you and your colleagues to the changes and challenges ahead. During the workshop part of the activity we will help you to identify the specific challenges your organization faces as it transitions to MDR.