We provide you a personalized support of our team of experts to help you maintain the CE mark on your devices
Implement innovative methodology and technology
To optimize time, recruitment and cost
With quality and ethics
Roadmap services for clinical trials
The Medical Writing Team Support
Our medical writing department will support you in writing different documents related to the clinical evaluation to complete the technical documentation of your medical devices from different risk-classes throughout the device lifecycle. Our medical writers have profound experience with the new European Medical Device Regulation (EU MDR 2017/745) and are following the guidelines of the Medical Device Coordination Group (MDCG).