Med-Clinical is offering Clinical Operations, Biometry, Market Access, Regulatory and Medical Writing Services for Medical Device, In-Vitro Device and drugs

Personalized support via our experts,​ helping you navigate the transition to the European Regulations: ​MDR 2017/745, IVDR 2017/746 and Regulation 536/2014​
Quality management system and SOPs designed according to: ISO 9001-2015 standards, best practices ISO 14155-2020, ISO 20916-2019, ICH-GCP E6(R2)​

We can also help you submit your funding applications to obtain state aid (BPI, Ministry of Health,...) or respond to calls for tenders from associations (Medicen, Eurobiomed,...)

Medical Devices and In-Vitro Devices benefit from an extension for the regulatory change

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

We work with companies all around the world

From the Middle East to North America and Europe, companies in all sectors (implants, anti-infectives, software, vaccines) rely on us to help them grow.

Medical device manufacturers, Medtech companies, Pharma industries, In-vitro devices manufacturers putted their trust in our company.