Basel, Switzerland – We at Europe IT Consulting GmbH are thrilled to announce a significant milestone in our ongoing efforts to support medical device manufacturers with compliance and regulatory requirements. (more…)
Medical Device Market in China: Current Developments and Interesting Details The Chinese market for medical devices is experiencing dynamic growth and offers numerous opportunities for companies worldwide. Here are some…
Did you heard about "EUDAMED Master UDI-DI" ? Here are the latest news about it and why the Master UDI-DI is needed. The European Commission is amending Regulation (EU) 2017/745…
Understanding Eudamed, UDI, and MDR: A Guide for Medical Device Manufacturers In the medical device industry, compliance with regulatory requirements is crucial for ensuring patient safety and product quality. One…
Handlungsbedarf für Medizinproduktehersteller im Bereich UDI GUDID / EUDAMED Was für Lebensmittel heute bereits gilt, wird auch für Medizinprodukte Realität. Die Rückverfolgbarkeit muss sichergestellt werden, mit dem übergeordneten Ziel, die…
https://www.youtube.com/watch?v=5-3xiXmfjhg&feature=youtu.beLearn in this short video how our global UDI software solution helps you ensure a smooth and successful UDI implementation.
Find out here about the latest UDI Implementation Timeline for EUDAMED.
https://www.youtube.com/watch?v=vuK0Fj55x-U&feature=youtu.beWhat is UDI? What are the goals? Who is affected? How can UDI be successfully implemented?Learn all important information about Unique Device Identification for EUDAMED and FDA in this short…
We are proud to announce to our customers that the latest version of our UDI SAP add-on for medical master data management for FDA is now S/4 Hana ready.During the…
The new version of the HL7 Converter is here.In the current version 1.3.2 minor improvements have been made.In addition, unnecessary restrictions were removed when converting the source file.For example, an…