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Using Real-World Evidence in Drug and Device Submissions
$397.00
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Submissions and Approvals
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
Proving Comparability in Cell and Gene Therapy Development: Untangling FDA Requirements
$179.00
Organizing Data and Document Archives: Finding a Needle in a Haystack for FDA Inspections – Webinar Recording/Transcript
$287.00
Supply Chain Solutions: How the Pharmaceutical Industry Can End In-Bound Issue – Webinar Recording/Transcript
$287.00
Gene & Cell Therapy Regulation: Comparability and Other New Developments – Webinar Recording/Transcript
$287.00