GMPs for Dietary Supplements: 21 CFR 111 Subparts B, C and D

This course is 8-Hours. This dietary supplement internal auditing course will help you understand the fundamentals of auditing and how to conduct an internal audit focused on cGMP and other FDA requirements. The training incorporates internal audit best practices, regulatory requirements and information on turning internal audit findings into useful information. Requirements for 21 CFR 111, supplier programs and FSMA are incorporated into the content.
You’ll learn how to prepare, perform, report and close an audit and discuss the importance of using CAPA systems as a follow-up to your internal audit findings.

Dates: November 12-13, 2026   

Times:  1:00pm-5:00pm Eastern Time (Both Days)

Cost: $800.00

*Register 3 or more attendees from the same company under the "General Registration" type, 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.

The purpose of this training is to understand the requirements for the NSF/ANSI 455-2 Good Manufacturing Practice for Dietary Supplement Standard and how to implement them at your facility. The standard is based on 21 CFR 111 requirements, other regulations (normative references), retailer criteria, and industry best practices. The criteria in this standard were structured to follow a seven (7) systems approach. In this training we will discuss what you will need to prepare in preparation for an audit at your dietary supplement manufacturing facility.

 We will not be discussing the need for documented procedures and evidentiary records in depth as this is well documented within the standard as well as the prerequisite Dietary Supplement GMP Training and is always best practice.

The training is divided into two sections:

Section 1

• Context of the organization- this includes requirements for implementing a quality management system (QMS) as well as regulatory requirements.
• Leadership- this includes requirements for management to demonstrate commitment to the QMS, such as assigning roles and responsibilities throughout the organization. 
• Planning, which includes requirements for planning for the ongoing function of the QMS.

Section 2

• Support - includes requirements for management of resources for the QMS. This includes buildings and infrastructure, human resources, and control of documents.
• Operation - includes requirements on planning and creating of the product.
• Performance evaluation - includes requirements for monitoring the QMS and evaluation of the product.
• Improvement - includes requirements for taking corrective action for product or process nonconformities, and actions to make the QMS better over time.

Key Learning Objectives

• You will learn the structure of the NSF/ANSI 455-2 Good Manufacturing Practice for Dietary Supplements Standard, with a detailed overview of each section of the standard.
• You will learn the specific requirements of the NSF/ANSI 455-2 Good Manufacturing Practice for Dietary Supplements Standard.
• You will understand the intent of the required programs and elements of the 455-2 standard from the NSF/ANSI 455-2- ARG - Audit Requirements Guidance for Good Manufacturing Practices for Dietary Supplements.
• You will learn best practices on how to implement the required programs and elements of the standard.
• You will learn what documentation is necessary to demonstrate compliance with the standard at your facility.

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

Dates: July 15-17, 2026                 
Time:   1:00 PM to 5:00 PM Eastern Time
 
Cost: $1000.00
Course Prerequisites: None

*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.