Webinarübersicht
Freue Dich auf spannende Themen, viel Input, und Inspirationen für effizienteres Arbeiten.
In diesem Webinar zeigen wir praxisnah, wie Sie Qualitätsmerkmale direkt im CAD verwalten, Prüfpläne digital aufbauen und Änderungen über das PLM-System kontrolliert und nachvollziehbar verwalten.
Learn how organizations can leverage SMART standards technology to streamline their regulatory requirements management, from importing requirements directly from external databases to implementing them seamlessly into development projects.
Dieses On-Demand Webinar zeigt, wie mit Model-Based Definition (MBD) Produktdaten direkt im 3D-Modell nutzbar gemacht werden können.
Learn how avaWorkflow supports you in managing and using your documents and their templates efficiently – and fully digitalized!
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.