21 CFR 111 GMP Dietary Supplement in Spanish - Recorded Session
The FDA expects all companies that manufacture, package, or store dietary supplement products to follow 21 CFR 111, Current Good Dietary Supplement Manufacturing Practices (cGMP). Combining extensive industry experience and a concrete understanding of regulations with flexible and convenient training, this course provides a solid understanding of the cGMP and the responsibilities expected of various individuals and groups within the company. You will learn how to apply cGMP principles to specific situations.
The 21 CFR 111 GMP training is interactive, with hands-on exercises including case studies of recent warning letters. Bring your questions and be prepared to interact with the instructor and your peers in the industry.
This dietary supplement GMP training course provides an overview of subparts A-P of Regulation 21 CFR 111, including:
• Manufacturing master records/batch production records
• Quality Authority and FDA
• Warning letters
• How to make sense of complex regulations in an understandable and comprehensive way
• How to effectively turn regulations into real-world examples and scenarios delivering clarity and operational success
• How regulations can be applied to your organization cost-effectively
Please Note: Once you have completed your registration, you will have access to the recording for 30 days. A PDF of the presentation will not be available. A Certificate of Participation will be issued once the course assessment is successfully completed.
Costo: $499.00 USD
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