Curriculum
Course Description: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.
Includes English subtitles.Access Duration:Access to this course expires 60 days from the date of registration or until you mark the course ‘Complete’ – whichever occurs first.
Course Objectives:
- 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
Who Should Participate:
- Dietary Supplement Manufacturing Personnel
- Regulatory Affairs
- Quality Assurance Manufacturing and Production
- Packaging and Labeling
- Quality Control Laboratory Operations