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TGA’s Australian UDI Database: Deadline Update
Australia's healthcare landscape is on the brink of a transformative change with the imminent launch of the Australian Unique Device Identification (AusUDID) database by the Therapeutic Goods Administration (TGA). With the AusUDID set to go-live in...
Innovit Announces GDSN.cloud Solution
June 7th, 2022 — Innovit, the Product Information Management (PIM) specialists who enable Healthcare Providers and Medical Products Suppliers to deliver trusted product data for supply chain management and clinical performance optimization, today announced their GDSN.cloud solution enabling healthcare manufacturers to easily share accurate & validated product data to the GDSN.
PRESS RELEASE: Innovit and atrify Strengthen Partnership Accelerating Healthcare Manufacturers Ability to Manage and Share Accurate Product Content
San Francisco, CA (June 3, 2022) Innovit, the Product Information Management (PIM) specialists in enabling healthcare providers to deliver trusted data best practices in supply chain and clinical performance and atrify, a leading provider of...
Introducing Innovit’s EUDAMED Reference Center
As a medical device provider one of the biggest changes on the horizon will be the new EU requirements for product information, as well as the FDA’s GUDID compliance deadline for Class I medical devices. Even the most experienced companies...
Device Registration ‘is live’ for voluntary UDI data submission
Last week, the European Commission announced the successful launch of its EUDAMED “Device Registration” and “NBs & Certificate” modules (Production release “v2.0 - September version” was deployed). The EUDAMED UDI/Device Registration and NBs...
FREE Early Access to the EUDAMED Test Environment!
Innovit is Excited to Announce Our EUDAMED.cloud Test Environment! To the best of our knowledge, we are the only company offering free access to a EUDAMED testing environment for all medical device manufacturers – helping you stay ahead of the...
An Important Milestone for the Medical Device Community: EU’s MDR-day has Arrived!
After four years of transition followed by a global pandemic in 2020, we reached a regulatory milestone on May 26, 2021 for Medical Device manufacturers in the European Union – with Medical Device Regulation 2017/745 finally taking effect. Yesterday, being the date of application of EU Medical Device Regulation (MDR) marks an important event for the medical devices market.
EUDAMED State of Play – New Playground Available for EUDAMED Device Registration and NBs & Certificates modules
What’s New? EUDAMED go-live date is still scheduled for May 2022. But you may recall that in order to ensure a smooth and effective implementation, the EU Commission provides a “EUDAMED playground.” It’s currently available for both manual web-...
PRESS RELEASE: B. Braun goes Live with Innovit direct GUDID connector
San Francisco, CA (September 23, 2020) Innovit, a global software company specializing in UDI compliance, Global Data Synchronization (GDSN), Master Data Management (MDM) and Product Information Management (PIM) solutions, has announced today that...
PRESS RELEASE: Innovit and Atrify Renew Global Partnership
SAN FRANCISCO - May 5, 2020 - PRLog -- Innovit, a global software company specializing in UDI compliance (Unique Device Identification), GDSN (Global Data Synchronization), MDM (Master Data Management) and PIM (Product Information Management)...
COVID-19 – An Update for Our Customers
Together, we face an unprecedented global coronavirus pandemic (COVID-19) and its impact on our families, businesses and communities. As we continue to monitor the rapidly evolving situation around COVID-19, our first thought is for the health and...
EUDAMED Playground M2M Testing – Success for Innovit!
We are so proud to announce that after the initial round of EUDAMED Playground M2M Data Exchange testing, Innovit was the only solution provider able to successfully complete all the test cases for Device/UDI Registration. Those test results were...
PRESS RELEASE: INNOVIT Expands Internationally with the Opening of Two New European Offices
San Francisco, CA (September 5, 2019) Innovit, a global software company specializing in Master Data Management (MDM), Product Information Management (PIM), Global Data Synchronization (GDSN) and UDI compliance solutions, has announced their plans...
Press Coverage: Dataversity – Master Data Management for Achieving GDPR Compliance
Innovit's Bruck Assefa talks to Dataversity about how to achieve GDPR Compliance with Master Data Management (MDM). http://www.dataversity.net/master-data-management-achieving-gdpr-compliance/
Press Coverage: New Kerala – Innovit Grows Global Healthcare Practice with Key Customer Wins
Reaffirming our strong presence in the healthcare industry by adding new customer implementations. https://www.newkerala.com/news/read/41287/innovit-grows-global-healthcare-practice-with-key-customer-wins.html
Press Coverage: Dataversity – Myths and Facts about Master Data Management (MDM): Part II
Innovit's Bruck Assefa talks to Dataversity about the myths & facts surrounding MDM. http://www.dataversity.net/myths-facts-master-data-management-part-ii/
Press Coverage: Becker’s Healthcare ‘Easing the pain of data integration for hospitals and manufacturers’
Innovit's MDM and PIM solutions in featured article from customer Becker Healthcare.
PRESS RELEASE: KMWorld: Innovit Releases Solution to Help Meet Regulatory Compliance
Innovit, a global master data management solution provider, is releasing the Unique Device Identification (UDI) Multi-Connector solutions, helping medical device manufacturers keep pace with regulatory compliance standards....
Press Coverage: Dataversity: Innovit Helps Medical Devices Manufacturers Meet Regulatory Compliance, Reduce Counterfeiting
http://www.dataversity.net/innovit-helps-medical-devices-manufacturers-meet-regulatory-compliance-reduce-counterfeiting/
Dataversity – Myths and Facts about Master Data Management
Myths and Facts about Master Data Management Dataversity http://www.dataversity.net/myths-facts-master-data-management/