Medical device manufacturers aiming to enter the EU market must fulfil the requirements of Regulation (EU) 2017/745 for attaining the MDR Medical device CE Marking for their devices. One of the ...

Docling uses state-of-the-art models for layout analysis and table structure recognition to transform unstructured documents ...

Abstract: The incorporation of sustainability principles during the requirements engineering phase of the development life cycle constitutes greening software requirements. This incorporation can have ...

Abstract: Changes in requirements occur throughout the software process from elicitation and analysis requirements through the operation of the software. Requirements traceability makes it possible to ...

The CRA imposes a sweeping set of cybersecurity mandates on manufacturers of digital products, including industrial equipment ...