Webinar Overview
Look forward to exciting topics, lots of input and inspirations for more efficient work.
In this webinar you get an overview of the new SMART standard format and existing services for the automated import of regulatory information from an external database. Moreover, the potential of AI and Large Language Models (LLM) are discussed. Last but not least, it is demonstrated, how the individual information units of a standard can be evaluated in a digitalized way, followed by efficient integration and traceability in requirements engineering as well as verification and validation documentation.
In this webinar, we will introduce you to the new features in avaClinical 2.0 and their benefits.
In this webinar find out more on how avasis and their Polarion products can help you implementing state-of-the-art digitalized processes in the medtech industry.
It's no secret: One of the biggest challenges in product development are "silos" of information. They arise from processes that are not interlinked and specialist process teams that are not able to exchange information efficiently
Regulatory requirements for clinical evaluations of medical devices increased over the last years. An important tool to reduce time and labor are software solutions for digital documentation.