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Webinar: From UDI to GDSN: How The Medical Device Data Landscape Keeps Evolving


Webinar: From UDI to GDSN: How The Medical Device Data Landscape Keeps Evolving

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Join John Lorenc from Reed Tech, Becky Aldhizer from STERIS Corporation, and Scott Brown from 1WorldSync as they discuss commercial data exchange efforts through GDSN. WATCH NOW FOR: The basic principles of GDSN and how it works How STERIS Corporation pivoted from UDI compliance to commercial data exchange efforts Best practices for collecting, storing, managing […]

Don’t Forget—Medical Device Data Submission Deadlines in 2018

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Beginning in September of 2014, medical device manufacturers have faced a series of data submission and maintenance requirements from the FDA as part of its Unique Device Identification (UDI) initiative. The agency phased the compliance deadlines by device class, requiring the highest risk device records to be submitted first to its Global Unique Device Identifier […]

Webinar: EU MDR’s Impact on Labeling: UDI in Europe and Other Changes

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Gary Saner of Reed Tech and Mark Cusworth of PRISYM ID discuss the new EU Medical Device Regulation (MDR) and In Vitro Diagnostics Regulation (IVDR), and the impact on labeling, including label formats, IFU information and symbols. WATCH NOW FOR: Label requirements comparison EU MDR vs MDD and AIMDD Comparison of EU MDR & FDA UDI […]

Webinar: Harmonizing your EU MDR Efforts with FDA UDI

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Gary Saner and John Lorenc of Reed Tech discuss UDI requirements in the EU and how device companies can align their EU compliance efforts with existing FDA UDI programs. WATCH NOW FOR: EU MDR / IVDR Overview EU UDI Requirements and Comparison to FDA UDI Global Data Management Approach Q&A Please complete the form to […]

Webinar: NHS eProcurement Requirements in 2018

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Gary Saner of Reed Tech discusses of what medical device companies need to do in 2018 to comply with the National Health Service eProcurement requirements and how affected medical device labelers can meet the deadline. WATCH NOW TO LEARN: UK NHS eProcurement requirements and timelines How eProcurement is similar to UDI, and how it’s different […]

A Joint Solution: Manage & Syndicate Device Product Data with Reed Tech & 1WorldSync

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Medical device professionals face an ever-growing list of demands for their product data from downstream users all over the world. Some of these demands are regulatory, such as FDA’s Unique Device Identification (UDI) submission mandate. Others are commercial, such as hospital networks needing access to device product data electronically through the Global Data Synchronization Network […]