RegMetrics simplifies the complex journey of medical device regulation for innovators, academics, and startups. Specializing in EU MDR and IVDR compliance, the platform guides users step-by-step through the regulatory process to help obtain CE marking and access UK and European markets. From initial device classification to generating GSPR checklists, RegMetrics translates legal requirements into straightforward questions, requiring no prior regulatory knowledge. In addition to its intuitive software tools, RegMetrics offers expert consultancy and training to de-risk development and accelerate market entry. It is the ideal partner for navigating medical compliance with confidence.
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