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.

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 product content solutions, announced today that they have strengthened their strategic partnership to accelerate global healthcare manufacturer’s ability to leverage […]

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 uncover critical gaps in their own internal systems and master data.   Under current timelines, a […]

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 curve for EUDAMED compliance. This new EUDAMED.cloud system is a cloud-based solution, serving as your […]

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 how they will affect the application of each aspect of MDR are outlined below:     Actor Registration Module – Already live. Device Registration (UDI) Module […]

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.

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- based user access, and an automated M2M (machine‑to‑machine) Data Exchange for Actor Registration, Notified Bodies (NBs) […]

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 B. Braun Medical Inc. (B. Braun) initiated its EUDAMED data submission project using Innovit’s UDI solution.  This comes after the team’s successful […]

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) solutions, has announced today that they have aligned on a global partnering agreement with atrify , a cloud-based platform for product […]