CORDIS Project
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EU4MEDTECH aims to streamline the regulatory process for medical devices and in vitro diagnostics by creating a comprehensive framework. This project will develop a digital platform to facilitate compliance and enhance the evaluation of clinical evidence throughout the product lifecycle.
The Medical Devices Regulation (MDR) and In Vitro Diagnostic Medical Devices Regulation (IVDR) have been introduced, replacing previous MD and IVD Directives to strengthen the EU regulatory framework, ensuring the highest levels of patient safety and smooth functioning of the single market for these products.
Yet, this regulatory update comes with challenges arising from the increased regulatory burden and strain across various actors in the EU HealthTech value chain.To overcome these hurdles, i…
SVEUCILISTE U SPLITU MEDICINSKI FAKULTET
Partner organizations (coordinator is shown above), with normalized type and CORDIS activity type. Guests see up to 4 partners.
Croatia, Split
Type: University / higher education
Activity type: Higher or Secondary Education Establishments
SME: No
Finland, SAVONLINNA
Type: SME
Activity type: Private for-profit entities (excluding Higher or Secondary Education Establishments)
SME: Yes
Ireland, Galway
Type: University / higher education
Activity type: Higher or Secondary Education Establishments
SME: No
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