Here’s a blog about the new GS1 Standard for Clinical Trials and how we can help you adopt it
Changing regulations, such as Annex VI clinical trial regulation, need to be incorporated into the label and artwork processes in time for when the regulation takes effect.
PRISYM ID will proudly be exhibiting at this year’s Pharma and Device Packaging and Labelling Europe event on 10th and 11th September 2019.
The imminence of Annex VI will have a resounding impact upon the clinical trial industry, adding further complexity to the existing compliance legislation.
Annex VI EU No 536/2014 is a clinical trial regulation which will impose new labeling challenges to the industry.
Are your current packaging and labeling processes preventing you from creating a faster, more flexible supply chain?
PRISYM ID will be both exhibiting and moderating at the Annual Medical Device and Diagnostics Labeling Conference in Chicago, US on 14th and 15th May 2019.
Barcodes are used by us all in everyday life, they are on every item we buy and use. However, many of us don’t know ‘what’s behind the lines’.
Release 1.8 of PRISYM 360 introduces new features to help medical device and clinical trials organizations to achieve complete label integrity and to meet the strictest FDA & EU regulatory requirements.
PRISYM ID will be exhibiting at the Clinical Trial Supply East Coast 2018 on the 16th and 17th of October, in King of Prussia, stand no 25.