HIBCC has announced the release of Beta version 2.3 of its ‘UDI Generator’ Utility. Learn how to create FDA compliant HIBC-UDIs online. Read Article ???
In recognition of the 20th anniversary of Pharmaceutical & Medical Packaging news, HIBCC CEO Robert A. Hankin weighs in on the advancements in automated identification technologies through the last two decades of their reporting. Read Article ???
What is a UDI and the GUDID? The Unique Device Identifier (UDI) is a system used to mark and identify medical devices within the healthcare supply chain. On September 24, 2013 the Food and Drug Administration (FDA) established a UDI system that requires manufacturers to include both a plain-text version of the identifying data, and […]
The following companies (and/or their subsidiaries/divisions) have applied for a Labeler Identification Code (LIC) assignment with HIBCC or one of our international affiliates. By doing so, they have demonstrated their commitment to patient safety and logistical efficiency for their customers, the industry and the public at large. Any organization that is interested in using the […]
The Food and Drug Administration (FDA) is proposing to establish a unique device identification system to implement the requirement added to the Federal Food, Drug, and Cosmetic Act (FD&C Act) by section 226 of the Food and Drug Administration Amendments Act of 2007 (FDAAA), Section 226 of FDAAA amended the FD&C Act to add new […]
