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Featured Product In Device Products

EU-MDR-Compliance-

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

Device Products

webinar recording

Organizing Data and Document Archives – Webinar Recording/Transcript

$287.00
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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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webinar recording

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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Labeling for Prescription Drugs, Biologics and Combination Products – Webinar Recording/ Transcript

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

$287.00
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Medical Device Warning Letters – Webinar Recording/Transcript

$287.00
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webinar recording

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

$287.00
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webinar recording

Using IT to Improve Data Integrity – Webinar Recording/Transcript

$287.00
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