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Featured Product In 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

Devices

Michael M. Gaba - blue 500

Medical Device Premarket Review Pathways and FDA Mechanisms for Expedited Review – Webinar Recording/Transcript

$287.00
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Califf's Post PDUFA - 600 red

Califf’s Post-PDUFA, Post-COVID FDA Agenda: Key Developments, Insights and Analysis – Webinar Recording/Transcript

$337.00
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Eric Henry - Blue 500

Medical Device Cybersecurity: Understand the Latest Developments – Webinar Recording/Transcript

$287.00
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Risks of Social Media Communication

Risks of Social Media Communication: A Guide to FDA and FTC Enforcement

$397.00
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James Pink - 600 Green

EU-MDR’s Growing Pains: Are You Current with the Latest Developments? – Webinar Recording/Transcript

$287.00
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Richard-Kingston-and-Diane-McEnroe-600red

Recall Readiness: Dust Off Your SOPs, There’s a New Guidance in Town – Webinar Recording/Transcript

$287.00
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Jessica Ringel -green600

Meet CDRH’s New Strategic Priorities: Where the Center is Headed and How Devicemakers Can Keep Up – Webinar Recording/Transcript

$287.00
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Pamela Forrest  -Aqua 500

Medical Device Reporting: Best Practices and Common Pitfalls – Webinar Recording/Transcript

$287.00
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Kristin Zielinksi Duggan Aqua 500

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

$287.00
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Kellie Combs and Josh-Oyster - 500blue

Communicating Directly with Consumers on Social Media: What You Must Know About FDA and FTC Ad and Promo Rules – Webinar Recording/Transcript

$287.00
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Kristen Grumet - Red

FDA’s New Quality Management System Regulation: What the Proposed Harmonization with ISO 13485 Means for Devicemakers

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David L. Chesney Aqua 500

Organizing Data and Document Archives: Finding a Needle in a Haystack for FDA Inspections – Webinar Recording/Transcript

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