FDA Quality Systems Regulation Requirements - Regulatory Documents Explained
1:10:24
FDA Requirements for Device Labeling
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Regulatory Documents Explained - DHF, DMR, DHR and TF
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How FDA Trains its Investigators to Review CAPA and What You Should Do to Prepare
57:00
How to Perform cGXP Assessment for Computerised Systems?
1:12:06
Medical Devices - ISO 14971 : Risk Management
1:13:50
21CFR Part 58 The Good Laboratory Practices GLP Regulation
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Design Controls - Requirements for Medical Device Developers
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