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PRISYM ID SPONSOR & KEYNOTE PRESENTER AT 4TH ANNUAL MEDICAL DEVICE GLOBAL LABELING STRATEGIES EVENT

We are a silver sponsor, exhibitor and presenter at the distinguished 4th Annual Medical Device Global Labeling Strategies Conference on 9 – 11 August 2016 in Minneapolis, US.

The conference addresses the industry’s drive to operate internationally, a complex process that requires organizations to implement a global labeling strategy and streamlined coordination. Speakers and delegates will discuss the latest insights surrounding international regulatory standards as well as benchmarking best practices in global labeling efforts.

Increasingly, global device manufacturers are realizing the importance of label lifecycle management when printing. Failure to streamline the labeling process can result in product recalls, damaged reputation and massive associated costs. Throughout the conference, we will be providing expert advice whilst exhibiting its label lifecycle management solution, PRISYM 360, which is created with the global ability to control labels centrally whilst simultaneously meeting country and regional needs with local variability and agility.

The conference will harness a variety of mediums including case studies, expert panels and interactive presentations to discuss key topics such as:
•    Enhancing the labeling process ahead of the impending global UDI requirements
•    Centralizing data storage to create control within labeling strategies
•    Adopting precise language that is easily translatable and culturally transferable

As one of the conference’s keynote presenters, our Sales Manager, Tim Fischer will host an interactive session on day #2 at 9:45am entitled: ‘Designing a Global Labeling Strategy given the Volatility of the Regulatory Climate’. The presentation will cover:

•    Predicting regulatory changes to anticipate organizational impacts and protect business needs
•    Intersecting regulatory requirements and organizational demands to advance labeling compliance protocols
•    Creating a User Requirement Specification (URS) foundation upon which to devise a global regulatory strategy
•    Start Your Engines: Leveraging regulatory rules engine to obviate compliance pitfalls and challenges

Tim comments: “The Medical Device Global Labeling Strategies event is an important opportunity for vendors and manufacturers alike. It offers the chance to share practical knowledge and advice on the current regulations and help the whole industry to prepare for the expanding global market.”

To arrange a meeting, book a place at PRISYM ID’s presentation slot or discuss your organization’s specific needs, please contact Tim Fischer via This email address is being protected from spambots. You need JavaScript enabled to view it.

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About the speaker:

tim-fischer Tim has spent over 25 years in and around Life Science compliance. Having launched his career at Abbott Labs in the Hospital Products Division in North Chicago, he spent most of his early days within Biological QA/QC as well as Small Volume Parenteral operations management. He then did additional technical work.

Following his Abbott days, he worked as Director of Compliance for 3 CMOs and in 2007 decided to strike out and perform 21 CFR 820 quality system consulting. It was during this period that he developed an appreciation for compliance software of which he has been heavily involved in over the course of 6 years including with PRISYM ID.

Tim lives in South Carolina where he and his wife thoroughly enjoy their time surrounded by 5 grown kids, 2 daughters in law and 2 year old granddaughter, Lilah Mae.