Innovit Announces GDSN.cloud Solution by | | News

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 by | | News

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 […]

Introducing Innovit’s EUDAMED Reference Center by | | News

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 […]

Device Registration ‘is live’ for voluntary UDI data submission on EUDAMED by | | News FREE Early Access to the EUDAMED Test Environment! by | | News

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 […]

EUDAMED Implementation and Roll-Out Timeline Update by | | News

The European Commission recently sent out an update on the plan for implementation and roll-out of EUDAMED, as it stands today. Changes to the implementation timeline of different modules, and […]

An Important Milestone for the Medical Device Community: EU’s MDR-day has Arrived! by | | News

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 by | | News

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 […]

PRESS RELEASE: B. Braun goes Live with Innovit direct GUDID connector by | | News

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 […]

PRESS RELEASE: Innovit and Atrify Renew Global Partnership by | | News

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 […]

See More News