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Using Real-World Evidence in Drug and Device Submissions
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Submissions and Approvals
The Biden Administration’s FDA: The First Six Months and What to Expect for the Rest of the Year – Webinar Recording/Transcript
$337.00
FDA’s Plan to Modernize the 510(k) Pathway: What Regulatory, Quality and Compliance Professionals Need to Know – Webinar Recording/Transcript
$287.00
Organizing Data and Document Archives: Finding a Needle in a Haystack for FDA Inspections – Webinar Recording/Transcript
$287.00
CDRH’s New Accreditation Scheme for Conformity Assessment: Impacts on Your Future Testing Plans and FDA Submissions – Webinar Recording/Transcript
$287.00
FDA Digital Health Regulation: Latest Developments for Medical Device Manufacturers – Webinar Recording/Transcript
$287.00
Medical Device Cybersecurity: Understand the Latest Developments – Webinar Recording/Transcript
$287.00
FDA Under the Biden Administration: What’s to Come and What It Will Mean – Webinar Recording/Transcript
$287.00
Maintaining Your Risk-Based Cleaning and Disinfectant Programs: Best Practices During COVID-19 – Webinar Recording/Transcript
$287.00