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So far UDIAdmin has created 9 blog entries.

The FDA’s UDI Compliance Mandate in Plain English – How We Can Help!

We formed UDI Compliance Solutions, LLC to help make the path to compliance easier and faster!

By |July 30th, 2015|UDI Compliance, UDI Solutions|

The FDA’s UDI Compliance Mandate in Plain English – The Label

The FDA UDI mandate calls for the placement of Device Identifiers (DI) and Production Identifiers (PI) on a UDI label.

By |April 8th, 2015|UDI Compliance, UDI Solutions|

The FDA’s UDI Compliance Mandate in Plain English – How Long?

The FDA deadlines serve to give medical device companies a target date to shoot for, however

By |March 30th, 2015|UDI Compliance, UDI Solutions|

The FDA’s UDI Compliance Mandate in Plain English – Who Benefits?

Unique identification is not a new concept, as the FDA has plenty of opportunity to draw on its experiences

By |March 25th, 2015|Uncategorized|

The FDA’s UDI Compliance Mandate in Plain English – Introduction

The premise on which the concept of a unique identifier is founded is far too important and far more complex than just having to label a medical device a certain way.

By |March 23rd, 2015|UDI Compliance, UDI Solutions|

UDI Compliance Solutions Software Free Demonstration

See a free demonstration of our proprietary software. The entire platform is designed as a cloud-based solution for all your UDI Compliance needs.

By |October 17th, 2014|Software Demonstration|

How Can UDI Compliance Solutions Help?

We take the guesswork out of the equation for our clients and improve your efficiency by freeing resources that can be better applied to your own core skill sets.

By |October 17th, 2014|UDI Solutions|

What Is UDI Compliance?

The Unique Device Identification (UDI) system mandated by the FDA is designed to protect patient safety and require the proper identification of medical devices.

By |October 17th, 2014|UDI Compliance|

UDI Compliance Solutions Answers

As the effective dates for UDI Compliance and enforcement edge closer there is suddenly a huge waive of information that is becoming available on a daily basis with regard to the suggested best practices and necessary filing requirements of the new FDA regulations and GUDID filing system. Unfortunately, as is often the case with documentation […]

By |March 25th, 2014|Charts, UDI Compliance, UDI Solutions|