Last week, Asphalion’s Medical Device Manager Francisco Rodriguez participated at the Medi’Nov Spain Conference with a talk about “The Regulatory Pathway to the Spanish Market”, reviewing the most important aspects of Spanish regulation focused on medical devices and especially medical software.
Key learning from Fran’s conference: “It is important to highlight that there are many software developments for which the qualification as medical devices and, if applicable, the regulatory compliance must be reviewed. Also, essential to be aware of local regulatory requirements where products are marketed.”
As the fourth-largest healthcare market in Europe and the leading country for the development of clinical trials, Spain has implemented a massive healthcare investment plan to meet the country’s needs and growing demand for innovative medical solutions and technologies.
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