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Featured Product In Devices

Selecting and Implementing Electronic Document Management Systems in the EU

Selecting and Implementing Electronic Document Management Systems in the EU

$197.00
Converting to an electronic document management system (eDMS) is key to increasing your record-keeping efficiency. Only one resource enables you to do that in a cost-effective manner while ensuring compliance with EU regulations: Selecting and Implementing Electronic Document Management Systems in the EU. Read More

Devices

Risk Management for Devicemakers

Risk Management for Devicemakers: New Requirements in ISO 14971

$397.00
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Implementing the IMDRF Codes – Webinar Recording/Transcript

$287.00
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Maintaining Your Risk-Based Cleaning and Disinfectant Programs – Webinar Recording/Transcript

$287.00
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Upgrade Your Medical Device Recall Strategy – Webinar Recording/Transcript

$287.00
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Evolving Quality Management Regulations

Evolving Quality Management Regulations: A Devicemaker’s Guide

$397.00
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Meeting Global Unique Device Identification Requirements – Webinar Recording/Transcript

$287.00
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Data Integrity in the COVID-19 Era and Beyond — Part I: The Impact of COVID-19 – Virtual Conference Recording/Transcript

$287.00
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Inspection, Measuring and Test Equipment – Webinar Recording/Transcript

$287.00
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Jon Gimbel

EU-MDR Postmarket Surveillance – Webinar Recording/Transcript

$287.00
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How to Address Medical Device Sample Size Issues – Webinar Recording/Transcript

$287.00
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Postmarket Surveillance Under EU-MDR

Postmarket Surveillance Under EU-MDR: Preparing for New Requirements

$397.00
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Usability Engineering: How the Updated ISO 14971:2019 Changes Your Process

Medical Device Safety in the Magnetic Resonance Environment – Webinar Recording/Transcript

$287.00
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