Med-Clinical is offering Clinical Operations and Medical Writing Services dedicated to medical devices manufacturers


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

Step 1 Define your protocol and create the study documentation​
Step 2 Identifying the participating sites
Step 3 : Manage the regulatory submissions and contract negociations
Step 4 : Monitor the study conduct and data collection
Step 5 : Ensure data quality, statistical plan optimization and writing reports, abstracts and articles

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).

All these steps are carried out in accordance with a quality process 

In using the ISO 9001 standards and ISO 14155

Details on our different provided services  

and made possible by our team of experts