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Home » Store » Regulatory Affairs

Featured Product In Regulatory Affairs

EU MDR Compliance: A Checklist for Meeting Manufacturing, Safety and Performance Requirements

$397.00
The FDAnews report EU MDR Compliance can help. Our editors have combed through the regulations, picking out the most minute compliance points and building them into a checklist of 200+ requirements you can use to confirm that you are satisfying all the EU mandates for device manufacturing. Read More

Regulatory Affairs

Medical Product Advertising & Promotion - Webinar Recording/Transcript

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Medical Device Calibration Program - Webinar Recording/Transcript

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How to Get IVD Approval Through CFDA - Webinar Recording/Transcript

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Compliance Confidence: Strategies for a Successful Regulatory Inspection

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510(k) Change Analysis: Complying with FDA’s Final Guidances

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Sensors and Wearables in Clinical Trials - Webinar Recording/Transcript

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Guide to FDA Regulation of In Vitro Diagnostic (IVD) Devices

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How to Build A World-Class Audit Team - Webinar Recording/Transcript

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510(k) Change Analysis - Webinar Recording/Transcript

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Medical Device Reimbursement Integration - Webinar Recording/Transcript

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Must-Know Contracting for Non-Lawyers - Webinar Recording/Transcript

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Expanded Access at a Crossroads - Webinar Recording/Transcript

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