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The European Medical Device Regulation (2021 Update e-book)

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$100.00

Risk Management Principles for Devices and Pharmaceuticals, Third Edition (e-book)

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$80.00

RAPS Webcast: Convergence 2026 Preview: A Conversation with Insiders (On Demand)

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$0.00

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Sponsored Webcast: Creating an FDA-Ready Moderator’s Script for your Human Factors Validation Study (On Demand)

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$0.00

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Sponsored Webcast: 15 Years of Labeling: What’s Changed and What’s Next (On Demand)

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$0.00

Certificate in Regulatory Writing

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$580.00

Sponsored Webcast: EU Deviations to IEC 61010-2-101: What IVD Manufacturers Need to Know (On Demand) (1 CE point)

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$0.00

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Software as a Medical Device, Second Edition (e-book)

From:
$80.00

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Software as a Medical Device, Second Edition

From:
$80.00

Sponsored Webcast : Common Pitfalls and Best Practices for Clinical Evaluation Submissions in The Fast-Changing MDR Environment (On Demand)

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$0.00

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Sponsored Webcast: AI Governance in Life Sciences: What You Need to Know About ISO 42001 (On Demand)

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$0.00

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Sponsored Webcast: How to Validate AI-Enabled, Non-Product Software (On Demand) (1 CE point)

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$0.00

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Sponsored Webcast: Three Truths and A Lie about Regulatory Submissions (On Demand)

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$0.00

Sponsored Webcast: Navigating Dual Compliance: A Practical Guide to Managing EU MDR and 510(k) Requirements in Parallel (On Demand)

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$0.00

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Sponsored Webcast: Scaling Accessible CTIS with Governed AI (On Demand)

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$0.00

Sponsored Webcast: The Unseen Risk Between MI and PV (On Demand)

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$0.00