FLYER | Software as a Medical Device by FDA (SaMD)

Understanding regulatory pathways for standalone medical software.

Understanding regulatory pathways for standalone medical software.

As digital health evolves, Software as a Medical Device (SaMD) is redefining how care is delivered — performing medical functions independently of hardware.

This flyer introduces SaMD concepts, FDA and IMDRF regulatory frameworks, and key considerations for risk categorization, quality management, and clinical evaluation.

Explore how SaMD supports innovation while ensuring patient safety and regulatory compliance.

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November 6, 2025
| By Hector

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