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
Program 2: UDI Gap Analysis and Recommendation
Program 3: UDI Implementation Management
Program 4: UDI Gap Analysis, Recommendation and Implementation Management
Program 5: UDI Gap Analysis, Recommendation, Implementation Management and Post-Implementation Follow-through
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…