WEBINAR 

Unique Device Identification (UDI) Updates for the US and Global Markets:

What dental manufacturers need to know

 

Recorded: Thursday, February 9, 2023, 11:00am EST

Register to view the live webinar brought to you by Reed Tech: Unique Device Identification (UDI) Updates for the US and Global Markets

UDI data requirement experts Gary Saner and Andrew Pfeifer of Reed Tech will discuss best practices for dental manufacturers to comply with current and emerging UDI and medical device registration mandates in the US and globally.

Reed Tech proudly supports the Dental Trade Alliance as a preferred UDI provider. 

In this webinar, we will cover the following subjects:

• UDI definition and goals
• FDA UDI requirements
• Label Data vs. GUDID submission data
• EU GUDID Compliance: Submission/Maintenance
• How Reed Tech can help

Bring your questions. We will also provide a table of the required data attributes and other key takeaways in the slides. Get started now! UDI preparation can be complex and time-consuming without subject-matter expertise.

Key Takeaways

For regulatory teams working on US FDA submission, this webinar will be a helpful walk-through of the main takeaways in the published information from the FDA and experienced guidance from the UDI ‘go-to’ specialists

Who Should Attend

• Regulatory Affairs/Operation Leaders
• Product Managers and Business Analysts
• Manufacturing, Operations, and Supply Chain Leaders
• Quality Leaders
• IT Support

Speakers

Gary 350x350

Gary Saner, Sr. Manager, Information Solutions Life Sciences, Reed Tech

Gary Saner is a subject matter expert on medical device unique device identification and other structured content reporting to regulatory agencies and commercial organizations. He has over 30 years of experience in software development, process management and data administration with the last 15 years focused on the life sciences industry. He serves as Co-Chair of the industry’s Structured Product Labeling Technical Team and on the Advisory Board of the Medical Devices Group.

ap

Andrew Pfeifer, Account Executive & Team Lead, Medical Devices

Andrew Pfeifer is a RAPS certified UDI global compliance expert, with many years of experience helping medical device organizations implement a sustainable and cost-effective UDI solution.

 

 

 

Register to review the recording and download informative slides. (Refresh your browser if this form does not appear)