Research and Development
Real-World Evidence in Medical Product Submissions: What Regulatory, Compliance & Quality Professionals Need to Know – 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
Organizing Data and Document Archives: Finding a Needle in a Haystack for FDA Inspections – 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
Gene & Cell Therapy Regulation: Comparability and Other New Developments – Webinar Recording/Transcript
$287.00
Recall Readiness: Dust Off Your SOPs, There’s a New Guidance in Town – Webinar Recording/Transcript
$287.00
CDER’s Priorities for 2022: What You Must Know About New Guidance and Program Plans – Webinar Recording/Transcript
$287.00