Mark Cusworth, PRISYM ID, examines The ten steps to labeling implementation for both SMEs and large enterprises – article published in Manufacturing Chemist
Barcodes labeling and packing are a critical part of the life sciences and medical devices products. However, how do you know that your barcode and packaging design surrounding it makes the grade? Read More
Medical device manufacturer, OriGen Biomedical, has selected PRISYM ID’s label management solution to put data at the heart of its medical device labeling processes.
Discover how PRISYM ID helped Origen Biomedical, a growing medical device manufacturer, who was looking for a cost effective and easy to use label printing process.
Whether you’re producing medical devices within Europe or supplying to Europe, as a manufacturer or supplier, you will need to adhere to the new EU MDR.
We like to make our webinars interactive and after our recent webinar on ‘EU MDR’s Impact on Labeling: UDI in Europe and Other Changes’, I thought it would be great to highlight the top five challenges and questions we saw strong responses to Read More
We are proudly sponsoring and speaking about EU MDR’s impact on labels at the 8th EU Medical Device Regulatory Affairs Conference 18-19 September 2018, in Brussels, Belgium.
PRISYM ID Professional Services is ideally suited to extending in-house labeling resources or providing access
to industry expertise that does not exist within the organisation.
With EU MDR deadline approaching and companies revising their MDR readiness, we are proudly speaking about the Operational Implementation of EU MDR Label Requirements at the 2nd Annual EU MDR Implementation Conference in Arlington, VA on 12-13 July 2018.
EU MDR introduces additional information that needs to be included on labels, forcing organizations to design new label templates that make room for data not previously part of the labeling system.
