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Video: Deeper Market Research with Reed Tech Navigator™ for Medical Devices


Video: Deeper Market Research with Reed Tech Navigator™ for Medical Devices

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Reed Tech Navigator™ for Medical Devices A whole new way to conduct deeper market research with safety and quality data. Learn more at ReedTech.com/Navigator Sign up for a demo of Navigator

Video: Informed Product Development with Reed Tech Navigator™ for Medical Devices

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Reed Tech Navigator™ for Medical Devices A whole new way to make data-driven product development decisions. Learn more at ReedTech.com/Navigator Sign up for a demo of Navigator

Video: Effective Post-Market Surveillance with Reed Tech Navigator™ for Medical Devices

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Reed Tech Navigator™ for Medical Devices A whole new way to conduct post-market surveillance analysis using device safety and quality data. Learn more at ReedTech.com/Navigator Sign up for a demo of Navigator

Video: Superior Risk Management with Reed Tech Navigator™ for Medical Devices

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Reed Tech Navigator™ for Medical Devices A whole new way to make data-driven risk management decisions for your device portfolio. Learn more at ReedTech.com/Navigator Sign up for a demo of Navigator

FDA Changes to Drug Listing Process for Contract-Manufactured Products

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The FDA recently introduced two significant changes to its process for drug listing products manufactured by contract manufacturing organizations (CMOs). It is important for CMOs and Private Label Distributors (PLDs) to understand these changes and make sure they update their internal processes in order to ensure successful drug product listing submissions going forward. Change #1 […]

Webinar: Harmonizing your EU MDR Efforts with FDA UDI

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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 Management Approach Q&A Please complete the form to […]