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
Latest Medical Device Postmarket Surveillance Requirements from China’s NMPA and the U.S. FDA – Webinar Recording/Transcript
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Data Integrity for Drug and Device Manufacturers: Avoiding Breaches and Closing Gaps
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Data Integrity in the COVID-19 Era and Beyond — Part III: The Real-World Costs of Data Integrity – Virtual Conference Recording/Transcript
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