Diego Rodriguez Muñoz
Diego Rodríguez Muñoz is a Clinical Research and Regulatory Associate specializing in medical device software, artificial intelligence, and biocompatibility. He holds a PhD in Molecular Bioscience and brings multidisciplinary experience across clinical research, regulatory affairs, and biomedical science. At MDx CRO, Diego supports clinical and regulatory projects for medical devices and in vitro diagnostics (IVDs), with particular expertise in the clinical and regulatory assessment of software-based and AI-enabled technologies, as well as biological safety and biocompatibility. He combines scientific expertise, data analysis, and regulatory documentation skills to support the development, evaluation, and market access of innovative healthcare technologies.
Latest Articles
Regulatory Updates
ISO 20417:2026: Medical Device Labelling Changes and Compliance Gaps
Last Updated: 2026-08-10
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Blog & Insights
EU AI Act and Medical Devices: What SaMD Developers Need to Know (2026)
Last Updated: 2026-08-10
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Blog & Insights
SaMD Compliance Guide: Navigating Regulations for Software as a Medical Device
Last Updated: 2026-07-28
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Blog & Insights
WHO Guidance for Digital Health (Nov 2022): Monitoring the Implementation of Digital Health
Last Updated: 2026-06-16
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Blog & Insights
Regulatory Updates