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AI REGU TOOLS

The AI Regu Tools support companies and organizations operating at the intersection of artificial intelligence and health technologies. They provide easier access to expertise, regulatory information, and support related to the EU AI Act and Medical Device Regulation (MDR), helping users navigate complex regulatory requirements, make informed decisions, and connect with relevant experts, networks, and collaboration opportunities.

AI & MDR/IVDR REGULATORY EXPERT DIRECTORY (FIN)

On this page, you will find a list of experts and service providers specializing in AI and MDR/IVDR regulation in Finland. The directory helps companies and organizations identify professional support, advisory services, and regulatory expertise related to artificial intelligence, medical devices, and compliance with applicable regulations.

AI & MDR/IVDR DEVICE REGULATORY PATHWAY TOOL

The AI & MDR/IVDR Device Regulatory Pathway Tool provides manufacturers with an overview of the key regulatory steps to consider when developing and placing an AI-enabled medical device on the EU market in Finland. It helps organizations navigate the requirements applicable throughout the device lifecycle, from development and conformity assessment to market access and compliance.

AI & MDR/IVDR REGULATORY EVENTS CALENDAR

The AI & MDR/IVDR Regulatory Events Calendar brings together events, training sessions, and webinars related to AI and MDR/IVDR regulation from a variety of organizers. The calendar also includes events organized by the AI Regu project, helping users stay up to date with the latest developments, learning opportunities, and networking activities in the field.