Webinar Overview
Look forward to exciting topics, lots of input and inspirations for more efficient work.
Learn how to integrate the Teamcenter Medical Device Solution (TC MDS) into your product development workflow. In our webinar, we’ll cover release processes, compliance tracking, and long-term version management. Discover how TC MDS optimizes workflows while ensuring regulatory compliance.
Discover how the system enhances transparency in approval processes by tracking who made, reviewed, and approved changes. Gain valuable insights into effectively utilizing these features to optimize your workflows and adhere to regulatory standards.
In this webinar find out more on usability engineering as product lifecycle processes within the quality management system, commonly unseen usability activities and their benefits, the important role of the task analysis, user interface specification and integration of clinical evaluation and post-market surveillance data.
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 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
Get a quick overview, which regulatory requirements are relevant for which products and easily integrate them into your product development process.