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INCREASING OPERATIONAL EFFICIENCY
With competitive pressure increasing, Life Science organizations are striving to improve time-to-market, whilst controlling operating costs.
This is leading the need to both streamline internal processes as well as remove any duplication of effort in processes, data and functions. Any paper-based processes may be intrinsically slow and subject to risk of errors.
Where systems or processes have been developed in local functions, there may be duplication of data or tasks, leading to repetition of effort, or more significantly, inconsistencies that lead to issues of quality or non- compliance.
How we helped one of our clients with this challenge:
- European Medical Device Manufacturer
- Sought to reduce waste from IFU over-production
- Implemented our print-on-demand solution
- Single language IFUs now printed at time of shipment
- Eliminating 175 tons of paper waste, saving $8M per annum.
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OFFERING THESE PRODUCTS AND SERVICES...
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.
INCREASING OPERATIONAL EFFICIENCY LABELING
Join medical device labeling and data experts from PRISYM ID and Reed Tech to learn about what the EU Medical Device Regulation (MDR) and In Vitro Diagnostics Regulation (IVDR) mean for labels in this free webinar.
The European medical device industry is in the grip of the biggest changes the market has seen in decades.