“Navigating AI Acts in Europe and the USA: Key considerations for MDR and FDA Approvals”

8 January 2025 | 4 – 5 pm (CEST) | Webinar

In this webinar, Jani Virtanen, Sales Director in MDS Finland, will examine the AI Acts in Europe and the USA, focusing on their impact on healthcare software and algorithm development. We will review the regulatory frameworks, highlighting key considerations for creating new healthcare solutions, and compare the regulations in both regions.

Key Takeaways:

- Overview of the AI Act in Europe and U.S. counterparts.
- Key similarities and differences in regulatory requirements.
- Important insights for developing AI tools in healthcare.

MDS Finland offers regulatory, quality management, and commercialization consulting for medical device companies. Jani brings extensive experience in navigating the regulatory landscape for medical devices.

SPARK Poland invites you to join our webinar on January 8th at 16:00 CEST.

Online via Zoom. Please register here by January 7 th. The webinar will be hosted by SPARK-Finland.

Please note that you will receive the meeting link and access code the evening before the lecture and that access to last minute registrations, cannot be guaranteed.