Ana Sofia Silva
Clinical Research Medical Device Regulation (MDR) Medical Writing

Ana Sofia Silva

Ana Sofia A. Silva is a Clinical Research Specialist with over nine years of experience in clinical research, project management, and medical writing for medical devices and in vitro diagnostics (IVDs). With a background in pharmacy and a PhD in neuroscience, she specialises in clinical investigations, performance studies, regulatory submissions, and clinical evidence generation under the EU MDR and IVDR. Ana Sofia combines scientific expertise with hands-on clinical operations experience to support the successful development and regulatory compliance of innovative healthcare technologies.

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