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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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  • Reed Tech Announces Agreement with GDSN Data Pool Solutions Provider 1WorldSync

    Reed Tech Announces Agreement with GDSN Data Pool Solutions Provider 1WorldSync

    This agreement will allow Reed Tech customers to access the Global Data Synchronization Network (GDSN) and provide 1WorldSync customers with expanded options for managing their regulatory data.

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  • FDA’s Electronic Drug Listing Requirements for Manufacturers

    FDA’s Electronic Drug Listing Requirements for Manufacturers

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  • National Drug Code (NDC) Assignment Guide eBook

    National Drug Code (NDC) Assignment Guide eBook

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

    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.”

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  • UDI Post-GUDID Publishing Webinar1:00:16

    UDI Post-GUDID Publishing Webinar

    UDI expert John Lorenc of Reed Tech examines post-submission UDI data maintenance and data management responsibilities and strategies.

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  • UDI Data Security: Why it should be important to you

    UDI Data Security: Why it should be important to you

    Data security has three facets—confidentiality, integrity and availability. Device labelers need to keep each of these areas in mind when it comes to managing the UDI data for their device portfolio.

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  • REMS in SPL Webinar1:03:44

    REMS in SPL Webinar

    SPL expert Gary Saner discusses the FDA's new initiative to receive Risk Evaluation and Mitigation Strategy (REMS) submissions in Structured Product Labeling format.

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  • Data Submitted! But the UDI Journey Continues...

    Data Submitted! But the UDI Journey Continues...

    September 24 and the Class II UDI deadline compliance date is past. But UDI is not over. For medical device labelers, it will always require maintenance and ongoing work. UDI is the new normal.

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  • 4 Reasons to Submit REMS in SPL Now

    4 Reasons to Submit REMS in SPL Now

    Some industry members may question whether REMS in SPL is worth the effort, since SPL is not yet mandated for REMS. Here are four great reasons to get start submitting REMS in SPL now.

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  • FDA Drug Establishment Site Registration Webinar31:30

    FDA Drug Establishment Site Registration Webinar

    SPL subject matter expert Jon Nolan gives an overview of the FDA's requirements for registering Drug Establishment sites. Learn More: http://www.reedtech.com/products-services/life-sciences/structur

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