Featured Product In Submissions and Approvals
FDA Oversight of Laboratory-Developed Tests — The Impact of the Final Rule
$249.00
Learn from a prominent regulatory expert how to optimize your LDT applications to help secure a 510k clearance or premarket approval. Read More
Submissions and Approvals
Califf’s FDA, 2023 and Beyond: Key Developments, Insights and Analysis – Webinar Recording/Transcript
$337.00
Medical Device Enforcement: Latest Developments from the FDA, DOJ and FTC – Webinar Recording/Transcript
$287.00
Impact of Artificial Intelligence and New Technology on Device Regulatory Compliance – Webinar Recording/Transcript
$287.00
Medical Device Cybersecurity: The Regulatory Landscape and How to Defend Your Practices During an Inspection – Webinar Recording/Transcript
$287.00
Fundamentals of FDA Inspection Management: Reduce Anxiety, Increase Inspection Success – Webinar Recording/Transcript
$287.00
FDA Pathways to Bring your Medical Device to Market: What Regulatory Professionals Need to Know – Webinar Recording/Transcript
$287.00
Building a World-Class Regulatory Intelligence and Support System – Webinar Recording/Transcript
$287.00