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  • NHS eProcurement Q&A19:55

    NHS eProcurement Q&A

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

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  • Reed Tech Navigator™ for Medical Devices Recognized with a 2017 Connectiv Innovation Award

    Reed Tech Navigator™ for Medical Devices Recognized with a 2017 Connectiv Innovation Award

    The Connectiv Innovation Awards recognize ground-breaking innovations bringing solutions to challenges seen within the B2B space.

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  • FDA Changes the Process for Drug Product Listings with No Updates

    FDA Changes the Process for Drug Product Listings with No Updates

    There are significant changes coming to the FDA’s electronic Drug Registration and Listing System (eDRLS) that require action from most drug labelers before the end of the year.

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  • NHS eProcurement Requirements, Timelines and Strategies50:51

    NHS eProcurement Requirements, Timelines and Strategies

    Join Gary Saner and John Lorenc of Reed Tech for a discussion of the UK National Health Service's eProcurement requirements and how affected medical device labelers can comply.

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

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

    eProcurement is a requirement for any organization doing business with an NHS care provider. For most device companies operating in the U.K., NHS is by far the largest customer in that market.

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  • Why the FDA Extended the Class I UDI Deadline (and What the Delay Means for You)

    Why the FDA Extended the Class I UDI Deadline (and What the Delay Means for You)

    FDA’s Class I extension is about ensuring GUDID data quality and submission accuracy, not about giving industry time to work on other projects.

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  • Structured Product Labeling, Eh? Health Canada’s SPL Pilot

    Structured Product Labeling, Eh? Health Canada’s SPL Pilot

    Health Canada is working with volunteer manufacturers and sponsors, as well as technology vendors, to test the application of the HL7 SPL standard to the content of drug product monographs.

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  • FDA Insight: UDI Data Quality

    FDA Insight: UDI Data Quality

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  • Why Data Accuracy in Drug Listings is Essential

    Why Data Accuracy in Drug Listings is Essential

    This month, FDA issued a warning letter to an OTC drug labeler for failing to provide complete and accurate information in the metadata sections of two drug listing files.

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  • GDSN for NHS eProcurement and Buyer Data Requests Webinar Reed Tech 1WorldSync1:01:26

    GDSN for NHS eProcurement and Buyer Data Requests Webinar Reed Tech 1WorldSync

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  • Despite Extension, 2017 UDI Deadline Still Holds for Certain Contact Lenses

    Despite Extension, 2017 UDI Deadline Still Holds for Certain Contact Lenses

    FDA delayed the UDI deadline for soft contact lenses to a future undetermined date but the September 24, 2017 deadline for rigid, gas-permeable contact lenses remains unchanged.

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  • Reed Tech Introduces GDSN Capabilities in Collaboration with 1WorldSync™

    Reed Tech Introduces GDSN Capabilities in Collaboration with 1WorldSync™

    The Reed Tech Life Sciences Team is pleased to announce that we are now offering a full-service solution to allow medical device organizations to share product data through the GDSN.

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  • Zoom In: A Closer Look at Device Safety Data

    Zoom In: A Closer Look at Device Safety Data

    There is a staggering amount of medical device safety data available from U.S. government sources. Where can we find it? What can it tell us?

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  • In the Spotlight: Medical Device Safety and Quality Events

    In the Spotlight: Medical Device Safety and Quality Events

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  • UDI Update: New FDA GUDID Technical Documents Released

    UDI Update: New FDA GUDID Technical Documents Released

    FDA sent an email to its list of UDI GUDID email subscribers with updated GUDID Data Elements Reference Table and GUDID HL7 SPL Implementation Files.

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  • Reed Tech® Introduces Reed Tech Navigator™ for Medical Devices

    Reed Tech® Introduces Reed Tech Navigator™ for Medical Devices

    Navigator is a new analytics and research solution that makes it easy to analyze and compare the safety and quality of tens of thousands of medical device products.

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  • Drug Product Annual Reporting Periods

    Drug Product Annual Reporting Periods

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  • GDUFA Self-Identification: What Generic Companies Need to Know35:25

    GDUFA Self-Identification: What Generic Companies Need to Know

    Reed Tech subject matter expert Jon Nolan talks GDUFA and Self-Identification during a webinar March 8, 2017.

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  • UDI & GDSN Webinar - Making the most of your GUDID Data1:00:56

    UDI & GDSN Webinar - Making the most of your GUDID Data

    GDSN expert Peter Alvarez of GS1 and UDI expert Gary Saner of Reed Tech discuss how medical device labelers can utilize the Global Data Synchronization Network (GDSN) to capitalize on their investment

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  • GDUFA and Self-Identification: What’s changing? (And What’s Not?)

    GDUFA and Self-Identification: What’s changing? (And What’s Not?)

    GDUFA requires sites engaged in certain generic drug activities to self-identify annually prior to paying a user fee set by the agency.

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