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
Dealing with FCPA and Other Investigations Under the New Normal – Webinar Recording/Transcript
$287.00
Medical Device Corrections and Removals, Recalls and Closures – Webinar Recording/Transcript
$287.00
Implementing Clinical and Performance Evaluation Reports for Your Medical Device – Webinar Recording/Transcript
$287.00
How to Manage Your Suppliers in China and India During the COVID-19 Pandemic – Webinar Recording/Transcript
$287.00
Using Monte Carlo Simulation to Aid Your Medical Device Design – Webinar Recording/Transcript
$287.00