Featured Product In Submissions and Approvals
Using Real-World Evidence in Drug and Device Submissions
$397.00
Acquire insights into the ideal RWE/RWD data to use in your product applications today with Using Real-World Evidence in Drug and Device Submissions. Read More
Submissions and Approvals
Gene & Cell Therapy Regulation: Comparability and Other New Developments – Webinar Recording/Transcript
$287.00
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
MDUFA Reauthorization Developments: What Regulatory, Compliance and Quality Professionals Need to Know – Webinar Recording/Transcript
$287.00
PDUFA and BsUFA Reauthorization Developments: What Regulatory, Compliance and Quality Professionals Need to Know – 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
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