Reduce product recalls associated with
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IS YOUR ROLE SUPPLY CHAIN?
When implementing a labeling system, your work dovetails with IT, and the solution you select must make the supply chain seamless to help you and your customers.
Rationalizing the process not only makes you and your team’s role easier, but as importantly has an affects your businesses bottom-line.
We provide a scalable Label Lifecycle Management platform that streamlines the production process, helping to reduce product recalls associated with labeling errors and the affect these have on profitability, resources and time.
Just-in-time and label postponement are just a couple of strategies that our solution facilitates and standardized labeling and streamlined manufacturing come as standard once our solution is implemented.
"The installation of PRISYM ID label software is the latest step in our ongoing effort to continually improve the quality of service we offer our customers. The recent upgrading of our packaging rooms, the expansion of our storage facilities and the enhancement of our IVRS capabilities are all important milestones for us and our customers."
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This solution provides organizations with complete label integrity to meet the strictest compliance requirements for FDA & EU regulations, specifically FDA 21 CFR Parts 11, 810, and 820.
SUPPLY CHAIN LABELING RESOURCES
EU MDR Labeling Compliance: Learn the Lessons from UDI. Date: 05 December 2017; 3PM GMT / 4PM CET
Whether you’re producing medical devices within Europe or supplying to Europe from the rest of the world, as a manufacturer or supplier, you will need to adhere to the EU MDR by May 2020.
READ OUR LATEST SUPPLY CHAIN LABELING BLOGS
- Survey reveals that only 17% of the respondents are aware of the changes that come with the EU MDR
- Sharing Knowledge & Experience in Label-Specific Challenges
- Clinical trials: when the label became more significant than the drug itself…
- Top three challenges in clinical trial packaging and labeling operations