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.
PRISYM ID, an SAP partner, today announced that it will participate at SAPPHIRE NOW® and ASUG Annual Conference being held June 5–7 in Orlando, Florida.
The PRISYM ID Lifetime Partnership Program is based around tiers of deployment models, from entry level Software as a Service (SaaS) right through to On Premise and Private Cloud.
During the webinar we had a couple of live polls, one of which was about the challenges the audience experience in achieving their labeling requirements Read More
