Top 9 UDI Compliance Challenges
Offered for One Day Only, Dec. 17, 2014 • At Your Convenience
Your Expert Presenters
Jay Crowley led the FDA team that wrote the UDI rule. As Senior Advisor for Patient Safety for CDRH, Mr. Crowley developed the framework and authored key requirements for the FDA's UDI requirements.
In December 2013, after a 27-year FDA career, Mr. Crowley became a VP of the UDI practice at USDM Life Sciences. USDM is a leading global professional services firm focused exclusively on providing business process, technology and compliance solutions for the regulated life science industry. USDM's professionals are recognized thought leaders in emerging life science computer system topics. They are experts in improving business value through the implementation and adoption of new technologies that run regulated business processes.
He wrote the UDI rule. Mark your calendar for Wednesday, Dec. 17, for On-Demand access to Jay Crowley’s webinar focusing on the top 9 challenges that devicemakers face in complying with the final rule.
Implementation is mandated in stages over the next few years, but truth be told, most companies are nowhere near compliance.
It's an on-demand webinar you can't afford to miss.
If you're like most device manufacturers, it's your first opportunity to get up close and personal with what the FDA is requiring of you in the coming years.
To help you, Mr. Crowley has identified the following 9 questions as the key challenges for the industry, and will provide implementation tips, best practices and in-depth answers to them:
It's no exaggeration to say that the FDA’s UDI rule impacts every device company and applies to multiple parts of each organization’s quality systems. This is not a rule that can be overlooked.
Sign up now to attend and you will also receive these invaluable documents to help with your company's transition to the new rule:
SPECIAL BONUS: Not sure your company will be ready by the FDA’s published deadlines? There is a way to apply for exemptions, extensions or alternatives, but you must understand the right way to approach the FDA. In this bonus take-away, Mr. Crowley will tell you how.
So, why not register NOW for Top 9 UDI Compliance Challenges: Former FDA UDI Chief Provides Answers? You'll get an insider's understanding of the complex nuances of UDI, detailed answers to your toughest questions and tips to help with implementation. If there has ever been a "must attend" webinar, this is the one! Sign up today.
Please note; this webinar has been previously recorded and no questions will be taken during the presentation. You may listen to the recording at your convenience on Dec. 17.
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