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The final day to register for this important training is Tuesday, March 19.
March 18, 2013
2 Min Read
This is a further reminder regarding the upcoming NSF training classes, offered in partnership with UNPA on March 26 to 27 and March 28. Please register now, as seating is limited. Please note all UNPA members will receive a 10 percent discount.
21 CFR 111 Dietary Supplement GMP Overview
About this course: This course provides attendees the tools necessary to successfully manage an inspection by the FDA. The FDA is actively auditing dietary all sizes of companies involved in the manufacturing, packaging, labeling, holding and distributing of dietary supplements.
Who should attend: This course is a must for employees at all levels involved with any activities associated with manufacturing, packaging, labeling or holding dietary supplements; as well as employees involved with the activities of quality control, quality assurance, packaging, labeling, and distributing dietary supplements in the U.S.
What you will learn:
The FDA inspection process in the context of producing and selling dietary supplements (or other FDA-regulated products)
Critical factors to consider and steps to accomplish well before any inspection ever takes place
How to effectively managing the process and issues that arise during the inspection to optimize the outcome
Essential elements of follow-up activities after an inspection to ensure a positive ending to this inspection and position your company for the next one
Location: Salt Lake City, Utah
Date: March 26 to 27, 2013
Learn more or register for this course
FDA Inspection Readiness Training
About this course: This course provides attendees the tools necessary to successfully manage an inspection by the FDA. The implementation deadlines for 21 CFR 111 have passed, and the FDA is actively auditing dietary all sizes of companies involved in the manufacturing, packaging, labeling, holding and distributing of dietary supplements.
Who should attend: This course is a must for employees at all levels involved with any activities associated with manufacturing, packaging, labeling or holding dietary supplements; as well as employees involved with the activities of quality control, quality assurance, packaging, labeling, and distributing dietary supplements in the U.S.
What you will learn:
The FDA inspection process in the context of producing and selling dietary supplements (or other FDA-regulated products)
Critical factors to consider and steps to accomplish well before any inspection ever takes place
How to effectively managing the process and issues that arise during the inspection to optimize the outcome
Essential elements of follow-up activities after an inspection to ensure a positive ending to this inspection and position your company for the next one
Location: Salt Lake City, Utah
Date: March 28, 2013
Learn more or register for this course
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