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...
