CEyoo GmbH

medical devices

About

Regulatory affairs, QM and market monitoring processes around the CE mark tie up a huge amount of capacity for some manufacturers. By taking over the manufacturer's responsibility, providing the process landscape and manpower for a proper QM system and ensuring professional market monitoring, CEyoo enables manufacturers to profit economically. And this is entirely in the interest of the Notified Bodies: Professionalism facilitates and accelerates the approval process and the medical device is on the market faster. CEyoo is a spin-off of Metecon GmbH in Mannheim. This means that CEyoo is backed by more than 20 years of experience in the areas of documentation, QM, market access and market monitoring, and more than 50 project-experienced contact persons with in-depth and wide-ranging expertise.

Technologies

Outlook Microsoft Office 365 Apache Mobile Friendly

Keywords

inverkehrbringen regulatory affairs marktbeobachtung fuer medizinprodukte marktzulassung qmsystem herstellerverantwortung qualitaetsmanagement und invitrodiagnostika qm startup klasse i klasse iprodukte ce zulassungsprozesse beschleunigen professionalitaet ivdr mehr als 20 jahre erfahrung mdr regulatory expertise post-market surveillance ivd regulation ivd medical devices eu-rep medical device regulation medical equipment and supplies manufacturing eu legislation product documentation notified bodies

Location

Mannheim, Baden-Wuerttemberg, Germany

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