Medical Device International Consulting Ltd
Country-specific Medical Device Regulatory Consulting
Our services
MDIC is a proven Regulatory partner, provides end-to-end Medical Device Regulatory services that span across decoding Medical Device classification
MDIC is a proven Regulatory partner, provides end-to-end Medical Device Regulatory services that span across decoding Medical Device classification, compiling Device documentation, Medical Writing, Device Registration and acting as an in-country representative.
With our presence across the continents, Medical Device International Consulting offers Regulatory services for market entry and Regulatory compliance across all regions.
Our dedicated team consist of a mixed pool of expertise offering one-stop solution for all the Regulatory needs.
Countries
With regional expertise and a deep understanding of local regulations, we deliver tailored solutions in:
Why MDCI?
MDIC is a proven Regulatory partner, provides end-to-end Medical Device Regulatory services that span across decoding Medical Device classification
Is a proven Regulatory partner
A team of 20 experts
Operates with regional expertise and a deep understanding
of local regulations
Our dedicated team consist of a mixed pool of expertise offering one-stop solution for all the Regulatory needs
Medical Device International Consulting Ltd
Adress: Suite 1, Second Floor, Sound & Vision House, Victoria, Mahe, Francis Rachel Street, Seychelles