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Featured Product In Medical 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

Medical Devices

BMDTEU Medical Device Trials in the EU: A Guide to the New EU MDR and Revised ISO 14155

Medical Device Trials in the EU: A Guide to the New EU-MDR and Revised ISO 14155

$397.00
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Effective Auditing for Manufacturing Quality webianr

Effective Auditing for Manufacturing Quality – Webinar Recording/Transcript

$287.00
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China’s NPMA (CFDA)

China’s NMPA (CFDA) – Webinar Recording/Transcript

$287.00
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01-22-20-Spreadsheet-Validation-Recording.png

Spreadsheet Validation – Webinar Recording/Transcript

$287.00
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Managing Data and Documentation for FDA Inspections

Managing Data and Documentation for FDA Inspections

$397.00
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Design Change Analysis

Design Change Analysis: Five Steps to Compliance

$397.00
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webinar recording

Organizing Data and Document Archives – Webinar Recording/Transcript

$287.00
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webinar recording

Increase Compliance, Reduce Risk with Integrated Digital Solutions – Webinar Recording/ Transcript

$287.00
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webinar recording

FDA 483s, Warning Letters & Enforcement Trends – Webinar Recording/Transcript

$287.00
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webinar recording

Understanding UDI in EU Device Regulations – Webinar Recording/Transcript

$287.00
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webinar recording

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

$287.00
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webinar recording

Develop World-Class SOPs that Minimize Human Error – Webinar Recording/Transcript

$287.00
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