Experts share advice on managing source data, local language labeling & country-specific requirements
Global medical device and life sciences product labeling is a complex subject and an integral part of the supply chain. The landscape is varied in terms of the systems and processes employed in designing, populating and printing labels (including booklets, inserts and IFUs). To control labeling on a global scale a number of key functions need to be managed including:
- Complexities around local language labeling
- Managing source data for labels, booklets, inserts and IFUs
- Customizing labels for country-specific requirements
Medical materials are shipped across many countries and many continents. For the sake of patient safety, the ability to control these materials’ labels at a global level is paramount. Labels must therefore be safely and accurately customized not only so that they are in the appropriate local languages, but also ensure country-specific nuances of including country-specific designs and regulatory requirements are understood sufficiently to communicate coherently with users.
Join us on 24th November 2015 for this information-packed session, where we explore what the industry can do to improve data security, adhere to regulations and mitigate the risks involved in local language labeling and country-specific design.
Latest blog - Mission Possible; Streamlining Label Validation. Read here.
Presented by
Craig Jones,
VP Enterprise Sales Engineering, PRISYM ID
Craig Jones is the Vice President of Enterprise Sales Engineering for PRISYM ID with responsibility for understanding customer needs and industry challenges to drive solutions to improve efficiency, minimise risk, address regulatory requirements and provide new approaches to business systems and processes. Craig has 14 years of experience delivering validated label lifecycle management solutions to life science and healthcare industries including medical device, pharmaceutical and clinical trial organisations. His experience includes roles as an industry consultant, in IT management and as a senior manager for global technical support and professional services.
Read our interview with Craig here.
Steve Ellison,
Business Development - Northern Europe, PRISYM ID
Steve Ellison has over 20 years' experience in the printing and coding business as well as several years consulting in the security and infrastructure software market. Steve joined PRISYM ID as the Business Development Manager for the UK, Ireland and Nordics where he is using his technical background and IT Skills to actively develop an understanding of the key benefits of Label Lifecycle Management solutions and in-line print inspection to the medical device and life sciences market.
Prior to PRISYM ID, Ellison held various managerial roles at Specops, Markem, Imaje and Systems Labelling.
