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.
The new modules recognise the constantly evolving operational and regulatory requirements life sciences and medical device organisations face.
PRISYM ID today announces the addition of two new modules to its flagship solution, PRISYM 360, to further transform global Label Lifecycle Management in the clinical trials and medical device industries.
The addition of these new, innovative modules comes in recognition of the ever-evolving operational and regulatory requirements life sciences and medical device organizations face. Each addresses specific data management and workflow needs to help ensure operational efficiency in the face of ever more complex global compliance demands.
Integrated, automated print inspection for Medical Device and Clinical Trial Labeling.
PRISYM 360 Vision to help remove risk of print errors, reduce costs and ensure compliance
We are announcing the general availability of PRISYM 360 Vision, a new automated print inspection module for our flagship PRISYM 360 labeling platform. PRISYM 360 Vision delivers the industry’s only label lifecycle management software to be fully integrated with print inspection hardware, reducing costs and removing risk whilst ensuring regulatory compliance.