In this webinar, industry experts from Siemens Digital Industries Software and PRISYM ID discuss how standards-based interfaces in the global application landscape can make your labeling more efficient and agile. Speakers will dive into topics surrounding the best practices, compliance, control and integration of global labeling systems (GLS).
What you will learn from this webinar:
In a 2021 World Health Organization report, there are more than 130 countries that have a national medical device regulatory. This means that medical device manufacturers must navigate continuous regulatory change to different aspects of the product development process, such as labeling. If manufacturers fail to keep up to date on each of their products and their geographies, there is a large risk of noncompliance.
There are many factors that make integrated labeling systems even more important today:
Watch the webinar to learn why end-to-end labeling is critical in the medical device industry.
Siemens has built a medical device solution to support product data models in line with industry norms. To meet customer offering and printing expectations, Siemens has formed a partnership with PRISYM ID in two key areas:
The first area focuses on the specialization of label authoring to support UDI and label content definition re-use. This is an integrated PLM and GLS solution to couple UDI records and label data management to GLS authoring and production specification capabilities. The second area focuses on cooperation of print inspection management through GLS into production control as record keeping of the MES system.
Watch the webinar to learn more about the bigger picture when it comes to aligning medical device solutions.