PITTSBURGH--(BUSINESS WIRE)--Rimsys, a world-leading Regulatory Information Management (RIM) software platform for medical technology companies, announced the release of an innovative and automated ...
A mandate for manufacturers to register their devices or in vitro diagnostics (IVD) in a new database for medical devices in Europe is on the horizon. The European Commission (EC) has outlined six ...
Distributors are not required to register in Eudamed but may be required to do so in accordance with Member State requirements. The Commission further noted that legacy and regulation devices where ...
UDI Connect addresses a persistent gap in UDI processes: while many MedTech organizations have invested heavily in robust data validation and internal workflows, the final step, submitting data to ...
New solutions deliver enterprise-grade data access and streamlined EUDAMED compliance, driving smarter, faster decisions across the business Rimsys, the global leader in Regulatory Information ...
The EC's European Database on Medical Devices (EUDAMED) is conceived as a way of improving transparency and oversight of medical devices and in vitro diagnostics (IVDs) on the European market. Image ...
BAD HERSFELD, Germany, Sept. 15, 2025 /PRNewswire/ -- p36 GmbH, a leading provider of digital compliance solutions for the life sciences sector, today announces the official launch of UDI Connect, a ...
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