ArisGlobal

Webcast Replay: 2014

Unique Device Identifier (UDI) Guidelines Update and Possible Strategies

The Unites States Food and Drug Administration (FDA) released the final rule on September 24, 2013 that requires most medical devices distributed in the United States to carry a unique device identifier (UDI). It also applies to certain combination products that contain devices and to devices licensed under the Public...Read More »


RIMS - ERP Systems Integration: Possibilities and Benefits

Global regulatory compliance mandates continue to evolve rapidly and aim directly or indirectly to ensure the quality and traceability of medical products delivered to the market. To ensure patient safety regulatory authorities continue to work more closely in a global and harmonized environment. Some examples of regulations that are harmonising...Read More »