anteris associates are going to visit the Medical Device Forum at TÜV SÜD in Munich (19 -20 March 2019).
With the adoption of the European Medical Devices Regulation, all market participants will face massive regulatory changes:
- What will change in concrete?
- How must manufacturers prepare for the new regulations
- What consequences will the changes have for approval, processes, products and monitoring?
At the Medical Device Forum, representatives of the authorities, TÜV SÜD experts and medical device manufacturers will present the most important regulatory areas and possible concepts on how to efficiently implement the new regulatory requirements.
Meeting slots are still avaliable - don´t hesitate to contact us. We are looking forward to a great event!