This course is designed 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.

Who Should Attend?

QA/QC, regulatory and compliance, laboratory personnel, purchasing and production managers.

Date & Time: 10/27/2025, 8am-5pm
Location: South Pacific Ballroom D, Lower Level

$1000

The labeling and promotion of your dietary supplement products are the most visible ways that the Food & Drug Administration and the Federal Trade Commission can track your compliance with federal regulations. A perfect complement to “Dietary Supplement Labeling Compliance,” this course will go over in detail each type of permitted claim that is available to you and the criteria for making each one. We will cover FDA and FTC standards for substantiation. We will also go over how to build the substantiation for each claim that the FDA and FTC requires you to hold to ensure your claims are accurate and not misleading, and how you can avoid making implied claims which could lead to regulatory enforcement. Participants will learn how public knowledge of FTC and FDA enforcement actions affect business performance, enforcement/litigation trends and other responsibilities of dietary supplement manufacturers such as structure/function claim notification.

Attend this FDA and FTC Claim Substantiation Course if you work in: Manufacturing, Quality Control/Quality Assurance, Management, Laboratory Operations, Packaging and Labeling, Auditing, Suppliers and Distributors, Regulatory Affairs and Compliance, Other Technical Professional

Date & Time: 10/27/2025, 8am-4pm
Location: South Pacific Ballroom C, Lower Level

$1000

The purpose of this training is to understand the requirements for the NSF/ANSI 455-2 Good Manufacturing Practice (GMP) for Dietary Supplements Standard and how to implement them at your facility. For those wondering what is GMP? or what does GMP stand for?, GMP full form is Good Manufacturing Practice. GMP encompasses a set of guidelines that ensure consistent quality and safety in product manufacturing. This GMP standard, which aligns with Current Good Manufacturing Practice (cGMP) and good manufacturing practices in the dietary supplement industry, is based on FDA regulations, specifically 21 CFR Part 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 to ensure comprehensive GMP compliance in the dietary supplement industry. In this training, we will discuss how to prepare for an audit at your dietary supplements 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 for quality assurance and quality control. Manufacturing, Quality Control/Quality Assurance, Management, Laboratory Operations,Packaging and Labeling, Auditing, Suppliers and Distributors, Regulatory Affairs and Compliance, Other Technical Professional

Date & Time: 10/27/2025, 8am-4pm | 10/28/2025, 8am-4pm
Location: South Pacific Ballroom B, Lower Level

$1200

Dietary Supplement GMP Overview

Attend an extensive 2-day training course on 21 CFR 111, the current Good Manufacturing Practices (cGMPs) in manufacturing, packaging, labeling, or holding operations for dietary supplements. This course is geared to those individuals involved in the dietary supplement industry including: Manufacturing, Quality Control/Quality Assurance, Management, Laboratory Operations, Packaging and Labeling, Auditing, Suppliers and Distributors, Regulatory Affairs and Compliance, Other Technical Professional

These guidelines are intended to be applicable to dietary supplements as defined and covered by 21 CFR 111 but may also be applied to dietary ingredients and other components. The course provides an in-depth review of the regulation and provides case studies to review recent FDA Warning Letters initiated to Dietary Supplement companies for non-compliance with 21 CFR 111 GMPs.

Date & Time: 10/27/2025, 8am-5pm | 10/28/2025, 8am-5pm
Location: South Pacific Ballroom A, Lower Level

$1400

Compliance

It is up to dietary supplement manufacturers to ensure their supplement labels are compliant before they go to market, however the regulations can be confusing and difficult to interpret. Label noncompliance can cause your product to be considered misbranded and subject to Food & Drug Administration regulatory action. Learn about the regulations that govern dietary supplement labeling including what can be considered a dietary supplement, mandatory aspects on the principal display panel, Supplement Facts formatting, ingredient lists, and type of permitted claims, enforcement/litigation trends, and other responsibilities of dietary supplement manufacturers such as Adverse Event Reporting. The course is interactive, with hands-on exercises. Bring your questions and prepare to interact with the instructor and your peers in the industry.

This course is geared to those individuals involved in the dietary supplement industry including: Manufacturing, Quality Control/Quality Assurance, Management, Laboratory Operations, Packaging and Labeling, Auditing, Suppliers and Distributors, Regulatory Affairs and Compliance, Other Technical Professional

Date & Time: 10/28/2025, 8am-4pm
Location: South Pacific Ballroom C, Lower Level

$1000