21 CFR 111 Dietary Supplement GMP Overview - Intro (8-hours)

Dates

Times

2 days8-hours VILT

Location

Virtual Learning

Availability

Dates

Times

2 days8 hrs VILT

Location

Virtual Learning

Availability

Dates

Times

2 days8 hrs VILT

Location

Virtual Learning

Availability

About This Course

This course provides an overview of 21 CFR 111, the Dietary Supplement CGMPs. This abridged course includes an introduction to current good manufacturing practices (cGMPs), required product quality elements, documentation, investigations, and a brief overview of the relevant subparts. We will also review the proper way to execute GMP records, detail the personal hygiene requirements, examine the meaning of master and batch records for control of production, labeling and packaging, clarify the requirements of quality and describe the purpose of GMP rules, regulations, and FDA enforcement.

Key Learning Objectives

At the end of this course, you will understand the following:

As a part of maintaining compliance to 21 CFR 111, dietary supplement personnel must have GMP training on a regular basis.

Who Should Attend?

Attend this training if you work in:

  • Management
  • Manufacturing
  • Quality control/assurance
  • Packaging
  • Marketing
  • Laboratory operations
  • Auditing
  • Suppliers and distributors
  • Regulatory affairs

Additional Recommended Courses

ISO 22716 GMPs for Cosmetic and Personal Care Professionals

This course is 8-hours. The ISO 22716 GMP cosmetics training will show you how to identify regulatory non-compliances before they become an issue, minimizing risk while adding measurable value to the manufacturing process. This course has been updated with information from the U.S. FDA's draft guidance for cosmetics manufacturing, U.S. FDA's GMP Inspection Checklist for Cosmetics, and general requirements from the Modernization of Cosmetic Regulations Act (MoCRA) enacted in December 2022.

Learners will understand globally recognized ISO 22716 standards and the U.S. FDA’s draft guidance for cosmetics manufacturing.

This course is geared to those individuals involved in the cosmetics Industry including:

· Marketing

· Quality Control/Assurance

· Packaging

· Manufacturing

· Laboratory Operations

· Suppliers and Distributors

· Auditing

· Regulatory Affairs

· Sales

· Retailers

· Product Development

· Brand Holders


Day 1: July 24, 2024

Day 2: July 25, 2024

Time: 1:00 P.M. to 5:00 P.M. Eastern Time (Both Days)


Cost: $800.00


Register 3 or more attendees from the same company and receive a 10% discount off each registration

Attending NSF training sessions does not provide an advantage, nor is it linked in any way to the granting of certification. Course log in details will be sent in a separate email. Certificate of attendance will be issued upon completion of the course. Completion of the course means being in attendance 95% of the log in time.

Virtual Classroom Training
21 CFR 111 Dietary Supplement GMP Overview

This training course is 16-Hours split over 3-days. FDA expects all companies that manufacture, package, or hold dietary supplement products to follow 21 CFR 111, the Dietary Supplement CGMPs. This course provides a basic understanding of CGMPs and the responsibilities expected for various individuals and groups within the company. Participants will learn how to apply CGMP principles to specific situations. The course is interactive, with hands-on exercises including case-studies from recent Warning Letters.


As a part of maintaining compliance to 21 CFR 111, dietary supplement personnel must have GMP training on a regular basis.
Course Prerequisites: None

Date: December 10, 2025

Time: 12:00 pm to 5:00 pm Eastern Time

Date: December 11, 2025

Time: 12:00 pm to 5:00 pm Eastern Time

Date: December 12, 2025

Time: 12:00 pm to 6:00 pm Eastern Time

Cost: General Registration $1200.00

*Register 3 or more attendees from the same company and receive a 10% discount off each registration*

Attending NSF training sessions does not provide an advantage, nor is it linked in any way to the granting of certification.

Course log in details will be sent in a separate email. Certificate of attendance will be issued upon completion of the course. Completion of the course means being in attendance 95% of the log in time.

Virtual Classroom Training
Vendor Qualification and Audit Training

Vendor Qualification and Audit Training


Unless you intend to test every shipment of every component for every specification, you must qualify your vendors. But FDA does not provide much guidance on how to qualify vendors. This class is designed for to give people who want to improve quality in their facility and who already have a basic understanding of the Dietary Supplement GMPs, the knowledge and skills necessary to qualify suppliers. Since the evaluation of all types of suppliers often involves auditing, this course will incorporate a fresh look at the process of auditing and the skills and techniques necessary to get the most from these activities. The auditing skills and techniques learned in this course are independent of the type of auditing or the standard being audited. These skills and techniques will be useful when conducting internal audits as well as performing audits of suppliers

Day 1: September 18, 2025 1:00pm-5:00pm Eastern Time
Day 2: September 19, 2025 1:00pm-5:00pm Eastern Time

Cost: $800.00

Completion of the course means being in attendance 95% of the log in time. Attending NSF training sessions does not provide an advantage, nor is it linked in any way to the granting of certification. Attending NSF training sessions does not provide an advantage, nor is it linked in any way to the granting of certification.

Virtual Classroom Training