The Innovit Corporate Affairs team is a highly skilled and experienced group of professionals dedicated to revolutionizing Master Data Management. With over 150 years of collective experience in this specialized field, they have established themselves as industry leaders and innovators.
Comprised of regional experts from diverse backgrounds, the Innovit Corporate Affairs team operates seamlessly across various locations, ensuring a global perspective and clear communications of our solutions for clients worldwide. Each team member brings a wealth of knowledge and insights specific to their respective region, enabling them to understand and address the unique challenges and requirements of different markets.
At the core of the team’s capabilities is their profound understanding of Master Data Management. They have honed their skills through years of hands-on experience, implementing and optimizing MDM strategies for organizations across industries. Their expertise covers all aspects of MDM, including data governance, data quality, data integration, and data stewardship.
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...
It’s hard to believe we’re more than halfway through January! You should be thinking and planning for the FDA’s GUDID compliance deadline for Class...
With the new year almost upon us, the FDA's GUDID compliance deadline for Class I medical devices must now be met with urgency. September...
First things first. What exactly is a Data Flow Model? A data flow model is diagrammatic representation of the flow and exchange of data within a...
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.
Today, medical device manufacturers are facing a wide array of data compliance demands from healthcare providers, and national regulators including...