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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
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How to Manage Your Suppliers in China and India During the COVID-19 Pandemic – Webinar Recording/Transcript
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Core Processes in the Pharmaceutical Laboratory: EU GMP-Compliant Sampling and Handling of Substances
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Continuous Quality Improvement for Pharmaceutical and Medical Device Manufacturers – Webinar Recording/Transcript
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Risk Management for Drug and Device Manufacturers: A Guide to FDA Policies and Processes
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