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Global Data Synchronization Network

Global Data Synchronization Network

UDI & GDSN - Making the most of your GUDID Data

UK NHS eProcurement: The What, Who, Why and When

Reed Tech SingleSource™ for Medical Devices

Does UDI matter when it comes to Reimbursements?

Is your supply chain process prepared for reimbursement scenarios? Traditional Class I, II, III medical devices and even some ‘specialty’ accessories (like unique packaging mechanisms) need a product data management strategy that includes reimbursement considerations...

What is a GLN (Global Location Number)?

Global Location Number (GLN) How does the supply chain keep ‘order’ in identifying locations and functions? The identifying key to determine the ‘where’–physical/digital location and the ‘who’—a function and or legal entity is the GLN. Global Location Number...

Happy New Year! Holiday Schedule

Due to the impending December 31 deadline for Establishment Registration and Blanket No Change Certification submissions, we are currently processing an extremely high volume of SPL conversion orders. Accordingly, to guarantee delivery by December 31, we must receive...

Increase Your Corporate Value by Providing Product Data via GDSN

Why your product data needs to be in GDSN…NOW! If you manufacture medical devices, you know the challenges in managing accurate, current, and complete product data and sharing it with your trading partners. Your data consumers, both internal and external, trust your...

Video: Medical Device Industry Trends & Timelines

What trends are expected with Global Regulator UDI activity and anticipated timelines? Listen to a short excerpt on medical device industry trends and timelines from the recent webinar: From UDI to GDSN-Are You Ready?   Questions about how to put your UDI data to...

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

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,...

Webinar: Harmonizing your EU MDR Efforts with FDA UDI

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...

Webinar: NHS eProcurement Requirements in 2018

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...

NHS eProcurement Q&A

Gary Saner and John Lorenc respond to questions submitted during a recent webinar on NHS eProcurement. Submit your questions to...

UK NHS eProcurement: The What, Who, Why and When

If your organization markets medical devices in the United Kingdom, you may have heard about the National Health Service (NHS) eProcurement program. Sometimes loosely referred to as the “U.K. UDI,” eProcurement shares some traits with FDA’s UDI program, but is quite...

GS1, GTIN, GDSN–What do they have to do with UDI?

If you are involved in your organization’s compliance program for Unique Device Identification (UDI), you have probably heard a lot of “G terms” being thrown around, like “GS1,” “GTIN” and “GDSN.” But what do these terms mean and where do they fit in with FDA’s UDI...

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