Now part of the Veranex family
Medidee significantly expands Veranex’s European footprint while also expanding the scale and scope of our clinical studies.
Why Medidee
Medidee significantly expands Veranex’s European footprint while also expanding the scale and scope of our clinical studies.
Our Strategy
Medidee expands and strengthens regulatory affairs, clinical development, and quality assurance services and capabilities at Veranex. As a leading MedTech regulatory and quality service consultancy company, this acquisition increases Veranex’s ability to navigate the European Union’s Medical Device and In Vitro Diagnostic Device Regulations (EU-MDR/IVDR) space. These services, coupled with the global infrastructure of Veranex, expand expertise and resources for the benefit of our healthcare partners.
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Related Services at Veranex
Regulatory Consulting
Navigate complex regulatory pathways with expert guidance that helps move your device or IVD toward approval with confidence.
Quality Consulting
Build quality into every stage of development with practical systems and compliance support that stand up to scrutiny.
Clinical Research
Generate the right clinical evidence with tailored study strategy and execution built around your device goals.
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