PRISYM ID to exhibit at the Pharma & Device Packaging & Labeling Conference West Coast 2016
- Themes include enabling optimization of product packaging and labeling for streamlined end-to-end operations and compliance -
PRISYM ID, the leading provider of labeling solutions for the medical device and life sciences industries, is exhibiting at the Pharma & Device Packaging & Labeling Conference West Coast on 16th & 17th November 2016, San Mateo, CA, USA.
The conference represents a forum for the medical device, pharma and biotech industry to discuss the latest developments and opportunities around new technology and solutions for streamlining labeling programs and processes, and achieving compliance with the latest global regulations such as Unique Device Identification (UDI).
As part of its attendance at the event, PRISYM ID will present its flagship PRISYM 360 label lifecycle management platform, as well as its latest print inspection module, PRISYM 360 Vision. The solution facilitates efficient and effective global-scale labeling operations and addresses topics including:
- Deploying a system to coordinate international approval of updated labels
- FDA UDI rule and international UDI standards management
- Complying with country of origin and target country requirements
Furthermore, PRISYM ID experts will be on stand offering advice on key topics such as ‘how to apply LEAN methodology to labeling programs and technology’; ‘Just in Time Labeling’; and ‘how to enhance the documentation process and supply chain agility’.
As the regulatory landscape continues to evolve, medical technology is required to ease these challenges. In a recent survey, PRISYM ID found that only 40% of companies surveyed are confident they are ready for regulatory inspection. The conference provides the opportunity for medical device organizations to explore the latest generation of technology solutions, including vision systems, to help automate the labeling process, increase compliance and reduce costs.
Warren Stacey from PRISYM ID comments: “Labeling plays an increasingly fundamental role in the end-to-end medical device supply chain. Many expanding organizations are now either distributing products or opening production sites in multiple countries, which adds new complexities to the supply chain process such as local language labeling and both global and regional regulations and requirements such as UDI. The ability to customize labels at the point of print with approved regional requirements and built in inspection as part of a validated system, means the right label goes on the right product, limiting wastage, increasing agility and accelerating speed-to-market.”
“The Pharma & Device Packaging & Labeling Conference is therefore a valuable opportunity for the PRISYM team to mix with regulators and manufacturers to share knowledge. As exhibitor we will be available to meet and discuss with organizations to understand how PRISYM products can help to enable an efficient and streamlined process while ensuring full regulatory compliance both today and in future.”
To arrange a meeting or discuss your organization’s specific needs, please contact us at firstname.lastname@example.org.