Kaplan Eduneering: ARCHIVED WEBINAR:: Dietary Supplements: Implementation of FDA’s Current Good Manufacturing Practices

ARCHIVED WEBINAR:: Dietary Supplements: Implementation of FDA’s Current Good Manufacturing Practices

This 60-minute webinar provided details on the 21 CFR Part 111 regulations, under which the FDA began GMP inspections of Dietary Supplement manufactures in 2008.

We discussed FDA’s expectations as it relates to implementing production process controls, a quality control department, a customer complaint system, documented testing, batch and laboratory records maintenance, and change controls.

We reviewed the 16 subparts of Part 111, which include General Provisions, Personnel Physical Plant and Grounds, Production and Process Controls, Quality Control, Requirements for Manufacturing Operations, and more.

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ARCHIVED WEBINAR:: Dietary Supplements: Implementation of FDA’s Current Good Manufacturing Practices

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