by Innovit Corporate Affairs | Nov 7, 2017 | Blog, UDI
Getting to Good Data in the GUDID* The United States Food and Drug Administration (FDA) regulation mandates that UDI data for Class I medical devices to be submitted with an impending deadline of September 24, 2018. This has made medical device manufacturers on a...
by Innovit Corporate Affairs | Nov 1, 2017 | Industry News, News
Long-time partners, 1WorldSync and Innovit, have joined forces to introduce PIM Lite. PIM Lite is a pre-configured, entry-level PIM system which brings immediate value by improving product data management processes for suppliers. Fully installed, pre-configured PIM...
by Innovit Corporate Affairs | Nov 1, 2017 | Blog
Bang Chau: Answering the “how” question as GS1 standards are adopted across the NHS No one doubts that using GS1 data standards on pharmaceuticals and medical devices can lead to improved patient safety and increased supply chain efficiency across the healthcare...
by Innovit Corporate Affairs | Oct 21, 2017 | Blog, GS1
For brand manufacturers and suppliers, to achieve business efficiencies, they need to ensure that their products align with GS1 standards, and ensure product data is synchronised with trading partners via GDSN data pools such as the National Product Catalogue (NPC)....
by Innovit Corporate Affairs | Oct 14, 2017 | Blog, UDI
UDI (Unique Device Identification) was legislated by the FDA on 24 September 2013. Device manufacturers were warned that failure to comply with UDI submission requirements would prevent them from selling products in the United States. It’s been two years since the...
