Due to EU regulations (2017/745, Medical Device Regulation MDR), which will become valid from 2021, requirements for documentation of medical devices will be tightened. This includes classification rules (GMDN, UMDNS, CND, etc.), technical specification, accessories, interaction with other products, predecessor products, intended use, conformity assessment, clinical evaluation requirements, traceability, post-market data, and European database expansion.
MDR has doubled the documentation retention period from 5 to 10 years. All these measures have the consequence that digitization, in particular the management of product information in a centrally accessible database, with versioning and traceability, will become fundamental for manufacturers of medical devices. crossbase has strategically positioned the medical industry as a target group.
Type of company: Trading company / Sales organisation Industrial (manufacturing)
Branch of industry: Tools
Country: Germany
Location: 87437 Kempten
Country: France
Location: 95041 Cergy-Pontoise Cedex
Country: Austria
Location: 6600 Reutte / Tirol
Type of company: Industrial (manufacturing)
Branch of industry: Building elements & Materials
Country: Germany
Location: 35260 Stadtallendorf
Country: Switzerland
Location: 7537 Müstair
Country: Italy
Location: 39011 Lana (BZ)
Country: France
Location: 68110 Illzach
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Deutschland
crossbase mediasolution GmbH
Otto-Lilienthal-Straße 36
71034 Böblingen
+49 7031 9880-700
office@crossbase.de
Österreich
crossbase mediasolution GmbH
Konrad-Doppelmayr-Straße 15
6922 Wolfurt
+43 5574 64880-39
office@crossbase.at
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