Featured Product In Regulatory Affairs
FDA Oversight of Laboratory-Developed Tests — The Impact of the Final Rule
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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
Meeting Global Unique Device Identification Requirements – Webinar Recording/Transcript
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Data Integrity in the COVID-19 Era and Beyond — Part I: The Impact of COVID-19 – Virtual Conference Recording/Transcript
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Medical Device Safety in the Magnetic Resonance Environment – Webinar Recording/Transcript
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Dealing with FCPA and Other Investigations Under the New Normal – Webinar Recording/Transcript
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