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FAQs

UDI compliance best practices and GUDID filing are relatively new areas of medical labeling that have become necessary due to the mandate established by the FDA in its continued effort to provide the greatest possible level of consumer safety. The UDI Compliance Solutions team and our strategic partners have been studying UDI regulations and proper protocols for compliance since the earliest stages of the FDA deliberations. We have prepared our own white-papers to educate industry professionals and to facilitate  the dissemination of information from important organizations like GS1. You can learn more about our efforts by clicking this UDI Compliance Answers link.

UDI Compliance Solutions can provide you with simple software solutions or detailed personal support on all matters relevant to the UDI framework and GUDID platform. Our experienced staff can walk you through the  now required by the FDA for medical device labeling. You can contact us any time and we will gladly assist you via email, phone or your preferred method of correspondence. We work directly with many of the premier names in this field and can help you with for even the most complex UDI applications.

UDI Compliance Solutions is a full service strategic partner capable of managing your GUDID Filing procedures and UDI compliance best practices. We are aware that industry professionals benefit from collaboration with others in this field, and we are pleased to recommend the UDI Forum . The UDI Forum is a useful, informative and polite online community where you can ask questions, get preliminary answers or seek additional assistance with all FDA, UDI and GUDID related inquiries.

The Food and Drug Administration has released numerous documents about mandatory compliance with Unique Device Identification (UDI) and GUDID standards. The FDA website is a good place for seasoned professionals to find answers to key questions about the requirements imposed by the UDI policy and regulatory environment now in place.