Webinarübersicht
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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.
Discover how to overcome complex challenges in medical technology with Teamcenter Medical Device Solution. Optimize team collaboration, streamline project management, and enhance product development. Join our webinar to learn proven strategies for efficiency and success.
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.
This on-demand webinar highlights efficient regulatory information management, integrating data into Polarion with avaREGULATORY, and guiding your company to prepare for upcoming changes through SMART standards.
In this on-demand webinar, we will use practical examples from our projects to explain which questions you should ask yourself as early as possible, what needs to be decided when selecting a possible software solution, what you need to decide internally BEFORE starting a digitization project, and how you can ensure that, in the end, software is implemented that users are really happy with.
In this webinar, we will present you our new Polarion solution avaADVERSE, which was developed for a digitalized procedure for searches in adverse event databases and an automated interface to the FDA databases MAUDE and Recall.
A huge problem in the MedTech industry: The 𝗶𝗻𝘁𝗲𝗿𝗳𝗮𝗰𝗲 𝗯𝗲𝘁𝘄𝗲𝗲𝗻 𝗰𝗹𝗶𝗻𝗶𝗰𝗮𝗹 𝗲𝘃𝗮𝗹𝘂𝗮𝘁𝗶𝗼𝗻 & 𝗿𝗶𝘀𝗸 𝗺𝗮𝗻𝗮𝗴𝗲𝗺𝗲𝗻𝘁 𝗳𝗶𝗹𝗲, and in particular the 𝗯𝗲𝗻𝗲𝗳𝗶𝘁-𝗿𝗶𝘀𝗸 𝗱𝗲𝘁𝗲𝗿𝗺𝗶𝗻𝗮𝘁𝗶𝗼𝗻 section in the clinical evaluation report. We strive to bring more clarity into that topic and help you understand current struggles of medical device manufacturers and how you can handle those.