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Usually well informed sources shared today the news, that the EU Commission today mentioned a two year delay to the EUDAMED release. They are working on further definition of transitional measured for the MDR and IVDR implementation.

GS1 has been designated today by the European Commission as issuing entity for Unique Device Identifiers (UDIs)

The Pharma MES in Berlin is a platform for the exchange of knowledge for the development and use of manufacturing execution systems in the pharmaceutical, biotech and life science industries and is regarded as the industry’s trend radar.

The Republic of Korea now follows EU guidelines for the manufacture of active pharmaceutical ingredients

The EU just released a new version of the FAQ document.