Class II medical device labelers face a Sept. 24 compliance date for UDI.
However, many labelers don't know where to begin or are unsure if they are taking the right steps to achieve compliance by the deadline.
On February 25, Reed Tech UDI experts Gary Saner and John Lorenc answered questions on all things UDI in a live Q&A webinar. If you missed it or want to revisit the topics covered, you can download the presentation slides and access the video here.
Gary and John are leading UDI experts in the medical device industry and each have over 10 years of experience assisting Life Sciences companies with electronic submissions of regulatory data to the FDA.
Reed Tech approached the process by finding the best solution for my company—not the best solution for Reed Tech
Current customer, Information Services Project Manager at medical device manufacturer with over 100,000 Class III, II, and I submissions
Reed Technology and Information Services Inc. (Reed Tech), based in Horsham, PA, is a leader in data capture, conversion and content management. Reed Tech is a LexisNexis company; LexisNexis is headquartered in Dayton, OH. It is a leading global provider of comprehensive and authoritative legal, news and business information, as well as tailored applications.
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