FDA 21 CFR Part 820 eLearning

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E-Learning

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eLearning

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1

Learning Objective: Overview about guideline 21 CFR Part 820
Code of Federal Regulation of Food and Drug Administration (FDA)

Focus:

• purpose, scope, application area and general contents
• identification of specific requirement as per 21 CFR Part 820
• application of concepts for quality assurance

Duration: approx. 4 hours