QSR
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
Recall Readiness: Dust Off Your SOPs, There’s a New Guidance in Town – Webinar Recording/Transcript
$287.00
Meet CDRH’s New Strategic Priorities: Where the Center is Headed and How Devicemakers Can Keep Up – Webinar Recording/Transcript
$287.00
Medical Device Reporting: Best Practices and Common Pitfalls – Webinar Recording/Transcript
$287.00
