Featured Product In Submissions and Approvals
Using Real-World Evidence in Drug and Device Submissions
$397.00
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Submissions and Approvals
FDA in 2024 and Beyond: What Election-Year Changes Mean for Your Business – Webinar Recording/Transcript
$337.00
FDA Oversight of Laboratory-Developed Tests — The Impact of the Final Rule – Webinar Recording/Transcript
$287.00
FDA as a Development Partner: A New Approach to Product Review Meetings – Webinar Recording/Transcript
$287.00
FDA’s New Sterilization Pilot on Risk-Based Cleaning and Disinfectant Programs – Webinar Recording/Transcript
$287.00
Pharmaceutical Quality Risk Management and ICH Q9(R1): Navigating the Global Intersection of Principle and Regulation – Webinar Recording/Transcript
$287.00
Real-World Evidence in Drug and Device Submissions: What Regulatory, Compliance & Quality Professionals Need to Know – Webinar Recording/Transcript
$287.00
Califf’s FDA, 2023 and Beyond: Key Developments, Insights and Analysis – Webinar Recording/Transcript
$337.00