The next UDI Compliance deadline for Class 1 is September 24, 2020. We want to make sure you are prepared to meet those requirements and evaluate the breadth of products that impact your company.
Many medical device manufacturers, including Arthrex, have already had to prepare for FDA’s UDI and meet compliance dates for Class III and Class II devices. Many more medical device manufacturers are in the midst of preparing for the upcoming Class I compliance date in 2020.
Getting to Good Data in the GUDID*
We can prepare and validate medical device product information before the compliance deadline, giving you more time to focus on producing the quality products your customers and patients love.
Recently 1WorldSync attended the UDI Conference that took place April 24 – 25 in Baltimore. Our healthcare experts were present and offered UDI implementation strategies and identify a sustainable process to successfully publish product content to the GUDID!
Are you prepared for the next FDA-UDI compliance dates?
Join us for a compelling webinar with Innovit and Arthrex on May 8th at 11 am EST.
You will learn how:
- A ‘single source of truth’ can help you get to good data in the GUDID and generate value beyond compliance
- Arthrex, a leading orthopedic medical device company, implemented a global strategy with Innovit PIM and 1WorldSync Data Pool to successfully comply with the UDI regulation.
- To roll-out a global strategy for product data syndication with help from Innovit & 1WorldSync experts
*GUDID – Global Unique Device Identification Database