We are happy to officially announce that projektraum36 is now a partner of atrify, one of the world’s leading providers of product information data exchange. This cooperation enables us to offer MedTech companies a holistic end-to-end solution for both data
We are proud to announce that our new website p36.io is now live. Over the past few months we have constantly developed ourselves and our portfolio. For this reason it was very important to us to adapt our website as
We proudly announce that we achieved SAP certification as built on SAP® Cloud Platform with our UDI Platform solution. The UDI Platform enables medical device manufacturers to handle their UDI related governance and submission processes for multiple regulatory authorities and
Am kommenden Sonntag, den 06. September 2020 startet der alljährliche Lollslauf im Rahmen des Lullusfests in Bad Hersfeld. In diesem Jahr sind wir vom projektraum36 das erste Mal als Sponsor des Lollslaufs dabei. Normalerweise findet das Lullusfest in Bad Hersfeld
We are proud to announce that we are now one of GS1 Germany’s Solution Partners and thus also part of the global network of GS1. We are looking forward to speaking the “Global Language of Business” and working together to
The corona virus pandemic is currently changing our entire professional and private lives drastically. For us as a company, the top priority is to protect the health of our employees while ensuring ongoing operations. For this reason, we have developed
Im Geschäftsjahr 2019 haben wir uns dazu entschieden, im Rahmen unserer Weihnachtsgrüße auf Grußkarten und Geschenke für unsere Kunden zu verzichten und wie bereits in vorangegangen Jahren eine Spende für gemeinnützige Zwecke zu tätigen. Dieses Jahr durften unsere Kunden mithilfe
We are proud having been recognized as being one of the 20 most promising SAP Solution Providers in 2019 by the CIO Review magazine. Based on our focus on Life Sciences Industry and SAP Cloud Platform solutions, we took the
Manufacturers of Medical Devices must take action now in order to submit their Product Master Data to Unique Device Identification (UDI) Databases worldwide. After the US Food and Drug Administration (FDA) the EU will follow with its Medical Device Regulation (MDR), becoming