Whew. You got through the unique device identification (UDI) submission process.

But you’re not done yet.

In http://medgroup.biz/UDI-next-steps, John Lorenc from Reed Tech explains UDI doesn’t end with your submission to the FDA’s GUDID database.

“After submission, you’re required to keep your GUDID entries up to date and continue submitting new records as you add to your device portfolio.”

And told me, “Since manufacturers are doing the work anyway, they may as well use the UDI data downstream. Leading device labelers are using the data records they submit to the FDA to update their own internal processes and systems.

UDI data can even form the basis for a Master Data Management (MDM) system.”

On April 6, UDI expert John Lorenc will present how to make your submission to FDA, keep your data up to date, and capitalize on it downstream.

Join us at http://medgroup.biz/UDI-next-steps and, even if you can’t make the live event, we’ll record it and send it to you afterward.

Thanks, John.

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A PREDICTABLE and REPEATABLE SALES PROCESS for MEDICAL DEVICES

Another free webinar for your team: http://medgroup.biz/predictable-sales next week.

Medical Devices Group Advisory Board member Mike Sperduti will cover how to:
• Launch your new medical device and quickly ramp your sales
• Build the best database in your space
• Build a sustainable sales pipeline
• Dramatically lower your sales expense

Virtual seats still available at http://medgroup.biz/predictable-sales

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Discussions

What Doctors Want [Survey Results]
http://bit.ly/doctr-survey

Product classification scenario
http://bit.ly/Classifcation

Justify sample sizes
http://bit.ly/smple-sizes

Marketing Medical Devices to the Federal Government
http://bit.ly/mdev-to-govt

Patient Engagement: What Is It Really?
http://bit.ly/pt-egmnt

How much reimbursement would I get?
http://bit.ly/reimb-amt

Are we seeing medical device tax repeal benefits?
http://bit.ly/tax-repeal-benefits

Device labeling question about manufacturer symbols
http://bit.ly/labeling-symbol

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Make it a great week.

Joe Hage
Medical Devices Group Leader

P.S. If you haven’t submitted unique device identifiers for your Class II and III devices yet, then you really really should attend the webinar. Click http://medgroup.biz/UDI-next-steps for the free content.

Alessio Domanda
Economia presso commerciale
Thanks for sharing UDI update.

Joe Hage
🔥 Find me at MedicalDevicesGroup.net 🔥
Here’s an alternate URL if you’re having trouble with the next-steps link: http://www.medicaldevicesgroup.net/webinar/udi-7/

An Nguyen
Director of Regulatory Affairs and Quality Assurance at IntraOp Medical Corporation
Hi Joe,
Thanks for sharing UDI update. I tried to bring up UDI-next-steps link but the page can not be loaded.

Best,

– An