Medical Device Manufacturers in the US have many questions as the Dec 8, 2022 GUDID compliance deadline approaches. This blog will answer some of the most common questions, and ensure everyone has the answers they need to begin their journey toward the FDA’s GUDID Class I Compliance.
Ashley Howell is the Marketing Director at Innovit leveraging 10+ years of experiences working for companies in the GDSN and PIM space working for companies including 1WorldSyncn and Kwikee. Ashley is passionate about democratizing data and product content to improve transparency among organizations.
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...
Start your Class I FDA GUDID data submission journey with these initial steps!
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...
Your New Year’s Resolution! Five easy steps for Risk Class I data submissions to FDA GUDID!
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...
Global UDI Syndication Hub: Comparing Two Data Flow Models
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...
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.