This recorded webinar provides an overview of the key elements of the cGMPs associated with personnel, physical plants and grounds, equipment and utensils, production and process control system, quality control, packaging and labeling, master and executed manufacturing batch records, laboratory operations, manufacturing operations, packaging and labeling operations, holding and distribution, records and record keeping.

Category: 

Dietary Supplements

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 involved with: Regulatory Affairs Quality Assurance Manufacturing and Production Packaging and Labeling Quality Control Laboratory Operations