Featured Product In Regulatory Affairs
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
Regulatory Affairs
Winning Device EU Marketing Approval: Seven Steps to Writing Clinical Evaluation Reports
$177.00
Navigating HCT/P Regulations: Risks and Opportunities for Drug and Device Manufacturers
$397.00