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Reed Tech Knowledge Center

Reed Tech, a LexisNexis company, is the provider of best-in-class information-based solutions & services to meet the needs of the global Intellectual Property market and key regulatory needs of the Life Sciences industry.

  • The USPTO’S EPQI and the Demand for Higher Patent Quality

    The USPTO’S EPQI and the Demand for Higher Patent Quality

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  • Three Ways Analytics Can Enhance Your Patent Prosecution Strategy

    Three Ways Analytics Can Enhance Your Patent Prosecution Strategy

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  • Patent Research Webinar | Free vs. Fee: How to Maximize for the Best of Both Worlds41:43

    Patent Research Webinar | Free vs. Fee: How to Maximize for the Best of Both Worlds

    Even if you use commercial patent research tools, you're likely still use free tools. How do you maximize your utilization of these tools to get the best of both worlds? We review coverage, results a

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  • Are you using the right law firm for your patent prosecution?

    Are you using the right law firm for your patent prosecution?

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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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  • How much will this Art Unit Cost to get a Patent?

    How much will this Art Unit Cost to get a Patent?

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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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  • Is it Time to Abandon that Patent Application?

    Is it Time to Abandon that Patent Application?

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  • Drafting Patent Applications to Overcome Alice Webinar1:01:59

    Drafting Patent Applications to Overcome Alice Webinar

    Listen as Ji'Nan Glasgow of Neopatents and Gene Quinn of IPWatchdog look at what these top companies are doing to be successful at overcoming Alice rejections. Review of the Big Four Blockbuster Elig

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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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  • Five Things to Look Out for in Choosing a Full-Text Patent Research Solution

    Five Things to Look Out for in Choosing a Full-Text Patent Research Solution

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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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  • Patent Research: Free vs. Fee

    Patent Research: Free vs. Fee

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  • TotalPatent One™: A New Solution for Patent Research

    TotalPatent One™: A New Solution for Patent Research

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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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  • No One is Above the Law

    No One is Above the Law

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  • The Anatomy of an National Drug Code (NDC)

    The Anatomy of an National Drug Code (NDC)

    An NDC is a 10 digit number that uniquely identifies a drug product by stringing together three separate code segments. A complete NDC is made up of a labeler code, a product code and package code.

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  • Drug Establishment Registration Reporting Requirements and Timelines

    Drug Establishment Registration Reporting Requirements and Timelines

    Every electronic drug establishment registration must be renewed or updated annually between October 1 and December 31, regardless of whether there have been changes to the data.

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  • UDI Data Submission Case Study: Henry Schein

    UDI Data Submission Case Study: Henry Schein

    As the Henry Schein team was faced with collecting...and maintaining all of this data for each product in U.S. distribution, they realized the process would be extremely time consuming.

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