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Register

Track: Regulatory, Quality and Good Manufacturing Practices

Focuses on the regulatory and quality aspects shaping medtech for those involved in regulatory affairs, quality management, or manufacturing.

[2025] [PLACEHOLDER] TBD – IMDRF

[2025] Innovation in Action: The Expanding Role of Real-World Evidence and In Silico Evidence

[2025] Innovations in Cancer Care Treatment

[2025] MDR/IVDR Implementation – A Reason to Believe?

[2025] Advancing Access: Regulatory Solutions for On-Label Pediatric Medical Devices

[2025] Setting Standards for the Future

[2025] Good Regulatory Practices and the Changing Brazilian Medical Device Landscape

[2025] AI and Automation in Promotional Review: Balancing Speed and Compliance for MedTech Innovation

[2025] Navigating the Regulatory Maze: Strategic Approaches to Cybersecurity Compliance in Medical Devices

[2025] Global Insights into Implementing Predetermined Change Control Plans

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