Med-Clinical is offering Clinical Operations and Medical Writing Services dedicated to medical devices manufacturers
OUR MISSION
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).