We've helped over 150 software and AI medical devices get to market. Harness regulatory and market access excellence through our consultancy services by experienced consultants and clinicians within the Software as a Medical Device (SaMD) and AI as a Medical Device (AIaMD) industry. We are a full stack consultancy: - Target Product Profiling and Value Propositions - Streamlined and agile FDA and CE/UKCA marking certification - Quality Management System design for software developers - Support against all ISO & IEC standards (13485, 14155, 14971, 62304, 82304, 27001, 42001 and more...) - Trained ISO auditors - mock audits and internal/external audit preparations - Notified Body and FDA engagement - Health economic modelling - budget impact and cost-effectiveness/cost-utility - Market access strategy and competitor analysis - Clinical evidence, clinical validation and post market clinical follow up - UKRP and PRRC functions - Intellectual property management - Investor due diligence Got a regulatory problem? We can fix it! Newsletter: https://www.hardianhealth.com/newsletter Contact us: https://www.hardianhealth.com/contact
