Dietary Supplements -- cGMPS for Manufacturing Plants and Equipment

The Final Rule (21 CFR Part 111) defines the current Good Manufacturing Practices (cGMPs) for the Dietary Supplement industry, including specific requirements for facilities and equipment. This course outlines current FDA requirements for facilities that manufacture, package, label, hold, and distribute dietary supplements. Topics in this course include: Physical Plant, Plant Design, Equipment and Utensils, and Records. After completing this course, learners will be able to identify FDA requirements for manufacturing plants and equipment that manufactures dietary supplements.

After this course learners will be able to identify fda requirements for manufacturing plants and facilities that produce dietary supplements identify fda requirements for sanitation, equipment, and utensils within those facilities identify fda regulations on record keeping for the manufacture of dietary supplements