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Featured Product In Quality

Biological Risk Evaluation and Management for Medical Devices

Biological Risk Evaluation and Management for Medical Devices

$397.00
Report shows how the FDA incorporates the two ISO standards in its medical device development policy, how the EU version of the two standards differs in significant ways and how the EU Medical Device Regulation may require further changes in the European standards. Read More

Quality

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

$287.00
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FDA 483s, Warning Letters & Enforcement Trends – Webinar Recording/Transcript

$287.00
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Understanding UDI in EU Device Regulations – 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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Develop World-Class SOPs that Minimize Human Error – Webinar Recording/Transcript

$287.00
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Medical Device Nonconforming Audit Findings – Webinar Recording/Transcript

$287.00
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Medical Product Off-Label Use and Marketing – Webinar Recording/Transcript

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Medical Device Warning Letters – Webinar Recording/Transcript

$287.00
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Transparency and the New Medical Device Reporting Rules – Webinar Recording/Transcript

$287.00
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Using IT to Improve Data Integrity – Webinar Recording/Transcript

$287.00
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The AI Revolution – Webinar Recording/Transcript

$287.00
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Clarity on Clinical Investigations – Webinar Recording/Transcript

$287.00
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