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UDI Implementation Consulting

FDA says Unique Device Identification will change the way medical device manufacturers or labelers operate… Patient Safety and transparency are now center stage.

DEADLINES are approaching! Is your company prepared to manage the requirements of this new regulation, which are far more reaching than implementation?

Contact us immediately to learn how we can help you manage this far-reaching change…

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FDA’s new UDI regulation will have a significant impact to medical device labelers now and in the future.  This outline of consultation programs addresses how RSQM Associates can help medical device labelers meet this new requirement and why it should be looked as an opportunity to help increase revenues, decrease costs and greatly improve their Master Data Management capabilities.


RSQM will also help you find the right company based n your needs to help with data synchronization to GUDID.  

RSQM UDI Implementation Programs

Program 1: One-day UDI Training Workshop
  • Learn about UDI and its impact on your company now and in the future
  • Download details on this Workshop

Program 2: UDI Gap Analysis and Recommendation
  • Understand the gaps that exist between your current systems and what is required to be compliant
  • Download information on our Gap Analysis program

Program 3: UDI Implementation Management
  • Oversee and manage your UDI implementation process
  • Download details on our Implementation Management

Program 4: UDI Gap Analysis, Recommendation and Implementation Management
  • Combines the two previous programs into one
  • Download information on this comprehensive program

Program 5: UDI Gap Analysis, Recommendation, Implementation Management and Post-Implementation Follow-through
  • Manages the entire process for our clients from gap analysis through post-implementation maintenance
  • Download details on our complete UDI implementation program
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