Featured Product In Postmarket Safety
FDA, FTC and DOJ Enforcement of Medical Device Regulations
$199.00
You can bridge the gaps within your organization, improve your ability to work with practitioners across all device-related fields, avoid enforcement actions and stay compliant. Let FDA, FTC and DOJ Enforcement of Medical Device Regulations show you the way.
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Building a World-Class Regulatory Intelligence and Support System – Webinar Recording/Transcript
$287.00
Engaging with the FDA: Best Practices for Dealing with Warning Letters, Seizures, Injunctions — and More – Webinar Recording/Transcript
$287.00
Real-World Evidence in Medical Product Submissions: What Regulatory, Compliance & Quality Professionals Need to Know – Webinar Recording/Transcript
$287.00
FDA’s New Quality Management System Regulation: What the Proposed Harmonization with ISO 13485 Means for Devicemakers – Webinar Recording/Transcript
$287.00
Organizing Data and Document Archives: Finding a Needle in a Haystack for FDA Inspections – Webinar Recording/Transcript
$287.00
Medical Device Premarket Review Pathways and FDA Mechanisms for Expedited Review – Webinar Recording/Transcript
$287.00
Califf’s Post-PDUFA, Post-COVID FDA Agenda: Key Developments, Insights and Analysis – Webinar Recording/Transcript
$337.00
Medical Device Cybersecurity: Understand the Latest Developments – Webinar Recording/Transcript
$287.00
EU-MDR’s Growing Pains: Are You Current with the Latest Developments? – Webinar Recording/Transcript
$287.00