From authoring through to submission, many Life Sciences companies struggle with maintaining a smooth and intuitive labelling process. Unconsolidated files and formats make it difficult for companies to track down and piece together relevant information, ever increasing the risk of error in end-results. And although there are many significant overlaps between the labelling process and other core RIM processes, why is it that we haven’t yet incorporated the Global Labelling Process into End-to-End RIM?
Join us for this webinar where Mark Willoughby, head of Life Sciences at Generis, will offer expert insight into overcoming the challenges of a disconnected Global Labelling landscape. See why the digitalisation of the labelling process as part of the end-to-end RIM process is so crucial.
Webinar Objectives:
- Understand the challenges of managing the global labelling process
- Recognise the cross-functional nature of labelling
- Utilising Structured Content Authoring to maintain quality and consistency of content
Reserve your spot today to discover how to manage your global labelling as part of your end to end RIM process.
Note : This webinar is from Mark's presentation at the GPRAS conference, it will cover the global labelling use case and will NOT include a demo of the CARA Life Sciences Platform.
