Who is Eumed®

Eumed® S.R.L was born in the early 2000s by will of Dr. Riccardo Dainese, sole director, with the aim of supporting medical device manufacturers in the complex process of CE marking and in the management of related regulatory obligations, including post-marketing surveillance.
Thanks to the collaboration with the lawyer Mauro Crosato, expert in health law and public administration, Eumed® has developed strong regulatory expertise, facilitating the interpretation of the complex rules of the sector. This synergy has led to the publication of books, participation in conferences and the training of professionals on Regulation (EU) 2017/745 and on Regulation (EU) 2017/746.
In addition to regulatory consultancy, Eumed® operates as an EU leader, managing the import and the verification of conformity of medical devices intended for the European market. Furthermore, it supports companies in the implementation of ISO 13485 and ISO 9001 quality management systems, in compliance with the organizational models of D.Lgs. 231/2001 and in participation in public procurement, including the MePA.
Since 2007 Eumed has been one of the main operators delegated to the registration of in vitro medical and diagnostic devices at the Ministry of Health and has become the reference point for communication activities of biomedical products to the competent authorities and for the rapid and correct assignment of Repertoire numbers to manufacturers, importers and distributors.
Through specialized training courses in Quality, Regulatory Affairs and Public Procurement, Eumed® contributes to the professional growth of companies and suggests commercial strategies to enhance the potential of products on the market.
Our team
dainese@eumedsrl.eu
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legal@eumedsrl.eu
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marketing@eumedsrl.eu
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itmedical@eumedsrl.eu
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diagnostics@eumedsrl.eu
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regulatory@eumedsrl.eu
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consulenza.eumedsrl@gmail.com