All Life Sciences Resources

  • Reed Tech® Introduces Reed Tech SingleSource™ for Medical Devices, Advancing the Ability to Manage and Share Device Product Data

    Reed Tech® Introduces Reed Tech SingleSource™ for Medical Devices, Advancing the Ability to Manage and Share Device Product Data

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  • You Missed the Drug Listing No Change Certification Deadline…Now What?

    You Missed the Drug Listing No Change Certification Deadline…Now What?

    If a drug product listing was not updated or certified in 2017 as containing no changes to the information on file, it has now been flagged in the NDC Directory as an uncertified product.

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  • Webinar: FDA's No Change Certification for Drug Products

    Webinar: FDA's No Change Certification for Drug Products

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  • FDA’s New Drug Product Listing Blanket No-Change Certification

    FDA’s New Drug Product Listing Blanket No-Change Certification

    Now, in addition to submitting updates to any product listings as they occur, drug product companies must submit a Blanket No Change Certification during the annual reregistration period.

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

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

    Manage & Syndicate Medical Device Product Data with Reed Tech & 1WorldSync

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  • Webinar: UDI and the EU MDR: What You Need to Know

    Webinar: UDI and the EU MDR: What You Need to Know

    Reed Tech Life Sciences and PRISYM ID team members discuss Unique Device Identification in the EU.

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  • Webinar: FDA Annual Reporting Period for Drug Products

    Webinar: FDA Annual Reporting Period for Drug Products

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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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