Expand your knowledge of key elements of cGMPs per 21 CFR Part 111: personnel, physical plants, equipment, production/process control system, quality control, packaging/labeling, manufacturing batch records, laboratory operations, manufacturing operations, packaging/labeling operations, holding/distribution, and records.

Subject area:
cGMP
Dietary Supplements & Herbal Medicines

Objectives (If applicable):
– Understanding the procedures and processes need to comply with FDA cGMPs in 21 CFR part 111
– Understanding the importance of and the means by which to comply with good documentation practices
– Understanding the importance of and the means by which to comply with meeting specifications

Target Audience (If applicable):
– Dietary Supplement Manufacturing Personnel
– Regulatory Affairs
– QA Manufacturing and Production
– Packaging and Labeling
– QC Laboratory Operations