Webinar Recordings
Real-World Evidence in Medical Product Submissions: What Regulatory, Compliance & Quality Professionals Need to Know – Webinar Recording/Transcript
$287.00
Drug Supply Chain Security Act Developments: What You Must Know About the Proposed Rule and Guidances – Webinar Recording/Transcript
$287.00
Orphan Drugs: Latest Regulatory, Compliance and Legal Developments – Webinar Recording/Transcript
$337.00
The FDA’s Focus on Clinical Data Integrity Throughout Product Development and Approval – 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
Pharmaceutical Process Validation: Best Practices for Success – Webinar Recording/Transcript
$287.00