International Clinical Evidence Professional Society, the global leader in the development of innovative approaches to evidence harmonization for medical devices and in-vitro diagnostics.
About MD-Clinicals
MD-Clinicals is a global Contract Research Organization (CRO) specializing exclusively in medical devices and in vitro diagnostics (IVDs). With more than 30 years of experience, we support manufacturers worldwide through clinical investigations, regulatory strategy, clinical evaluation, and market access, helping bring innovative technologies to patients faster and with confidence.
What they do
- Conduct global medical device clinical investigations and IVD performance studies.
- Develop clinical and regulatory strategies for worldwide market access.
- Prepare clinical evaluation and performance evaluation documentation (CER/PER).
- Deliver post-market clinical follow-up (PMCF) and medical writing services.
- Support manufacturers from product development through regulatory approval and commercialization
Why choose MD-Clinicals
- 30+ Years of Expertise – Dedicated exclusively to medical devices and IVDs.
- Global Reach – International clinical operations with experienced local teams.
- Regulatory Excellence – Proven expertise in MDR, IVDR, and global market access.
- Tailored Solutions – Flexible services adapted to each product and development stage.
- Trusted Partner – A strong track record of successful clinical investigations and regulatory submissions worldwide.
Why the support ICEPS
"At MD-Clinicals, we believe that advancing clinical evidence requires more than conducting high-quality clinical investigations—it requires a strong professional community. ICEPS brings together experts from across the medical device ecosystem to share knowledge, promote best practices, and shape the future of clinical evidence. Supporting ICEPS reflects our commitment to scientific excellence, collaboration, and ultimately improving patient care."