PRISYM ID, one of the leading providers of labelling solutions for the medical device and life sciences industries, is hosting a webinar about ‘implementing and achieving UDI compliance’ and whether the benefits of UDI have outweighed the pain.
The webinar takes place next Wednesday, on January 27, 2016 at 3pm GMT/10am EST, and is presented by leading experts Kevin Grygiel, VP of US sales, PRISYM ID and Gary Saner, senior manager, information solutions – Life Sciences, REED TECH.
Throughout the seminar, the company will address key points including: Identifying the main challenges of UDI compliance, and how manufacturers are working to meet them, and understanding how to make the labelling requirements more efficient, compliant and risk free.
Grygiel and Saner will discuss the impact of the changes on the medical device labelling landscape in the last couple of years following the introduction of UDI. In addition, they will consider how organisations can learn from UDI adoption to reduce risk, increase efficiency and meet regulatory requirements in the future.
For many organisations 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 organisations ascertain whether they are now ready for an FDA inspection, which includes assessment of UDI activities.
Grygiel commented: “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 organisations 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.”
You can register now for free: http://www.prisymid.com/how-the-gudid-was-it