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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

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The Inextricable Link Between Data Integrity and Quality Culture – Webinar Recording/Transcript

$287.00
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Dave Petrich-600green

Process and Design Validation for Devicemakers – Webinar Recording/Transcript

$287.00
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David L. Chesney Aqua 500

Fundamentals of FDA Inspection Management: Reduce Anxiety, Increase Inspection Success – Webinar Recording/Transcript

$287.00
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Manufacturing Quality: Using Audit Observations to Predict Problems – Webinar Recording/Transcript

$387.00
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Shelly Garg - Aqua 500

FDA Pathways to Bring your Medical Device to Market: What Regulatory Professionals Need to Know – Webinar Recording/Transcript

$287.00
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Clinical Data Integrity

Clinical Data Integrity: FDA and DOJ Enforcement Priorities

$397.00
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Dennett Kouri and Faviola Michelot - 500blue

Building a World-Class Regulatory Intelligence and Support System – Webinar Recording/Transcript

$287.00
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Steve Silverman -red600

Engaging with the FDA: Best Practices for Dealing with Warning Letters, Seizures, Injunctions — and More – Webinar Recording/Transcript

$287.00
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Paul Gadiock and Olivia Cusimano-500aqua

Charging for Investigational Drugs and Devices – Webinar Recording/Transcript

$287.00
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Kristin Zielinski Duggan, Lynn Mehler and Sally Gu

Real-World Evidence in Medical Product Submissions: What Regulatory, Compliance & Quality Professionals Need to Know – Webinar Recording/Transcript

$287.00
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Complying with the EU MDR

Complying with the EU MDR: New Guidances, Standards and Procedures

$397.00
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Beverly Lorell, Peter Leininger and Mark Brown - red 600

The FDA’s Focus on Clinical Data Integrity Throughout Product Development and Approval – Webinar Recording/Transcript

$287.00
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