© Copyright 2026, All Rights Reserved
Regulatory consulting for medical devices and diagnostics
Ensure compliance with MDR and IVDR regulations; Support clinical trials for medical devices; Assist laboratories in achieving ISO accreditation; Develop regulatory strategies for market entry; Facilitate CE marking and FDA approval processes.
Funded by the European Union - Next Generation EU; Specializes in AI and software as medical devices; Focus on innovation in health technology.
Main Information
Contact & Links
Key Information
Company Context