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UDI regulations kick in for Class I and II devices in 2015.
So let’s start the year with a free webinar for ways to make your UDI submissions easier.
Reed Tech is my go-to on this subject. They’ll cover:
• Requirements of a GUDID submission system
The live event is January 21 at noon Eastern Time but the video replay, slides, and transcript will be made available for all who register.
For today’s discussion, a question for the Class III manufacturers who submitted in 2014.
Do you advice to give the group from your experience? Maybe some “watch outs?”
We’ll take questions on the live call. Register at http://medgroup.biz/UDI-in-2015
SPEAKING OF WEBINARS
Did you know we archive each Medical Devices Group webinar for later playback?
See http://MedicalDevicesGroup.net/webinar for replays, slides, and transcripts for content dating back three years!
Most recent addition: Video/slides/transcript for “How Medical Device Websites are Evolving” at http://medgroup.biz/device-sites
Medtronic’s $63-million gift to executives
Your thoughts on connecting devices to smartphones?
How to get started in a start up?
Are “better outcomes” smoke and mirrors?
A good template for a Class I recall?
Will Sony finally scare you into action?
How to make a value analysis committee process easier?
Are device manufacturers concerned about packaging quality?
Does “Value” mean “Low Price” for Medtech?
Make it a great week.
P.S. Our Super Bowl pool. Winner gets one free 10x admission: http://medgroup.biz/superbowl
The UDI regulation for class II devices takes effect in 2016, not 2015. In fact, the FDA will not even accept applications until later this year so those companies can begin listing their devices.
The corrected statement, then:
I apologize for my error.
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