Press Releases


We are hosting a webinar about ‘Implementing and Achieving UDI compliance’ and whether the benefits of UDI have outweighed the pain. The webinar takes place on 27th January 2016 at 3pm GMT/10am EST and is presented by leading experts Kevin Grygiel, VP of US Sales, PRISYM ID and Gary Saner, Sr. Manager, Information Solutions – Life Sciences, REED TECH.

Throughout the seminar, we will address key points including:

  • Identifying the main challenges of UDI compliance, and how manufacturers are working to meet them
  • Understanding how to make the labeling requirements more efficient, compliant and risk free

Our speakers will discuss the impact of the changes on the Medical Device labeling landscape in the last couple of years following the introduction of UDI. In addition, they will consider how organizations can learn from UDI adoption to reduce risk, increase efficiency and meet regulatory requirements in the future.

For many organizations the journey to compliance has not been a simple path and many have had to make huge changes to their internal processes. The webinar will help these organizations ascertain whether they are now ready for an FDA inspection, which includes assessment of UDI activities.

PRISYM ID’s VP of US sales, Kevin Grygiel comments: “We’re excited to host our latest webinar on implementing and achieving UDI compliance and to support delegates with their understanding of the key topics. At PRISYM ID, we are committed to supporting organizations in the changing regulatory environment and helping them ensure patient safety. The latest webinar is our way of ensuring that our customers remain at the forefront of technology adoption through clear understanding of the issues they face today.”

Click here to register to our free webinar

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