Nutritional Supplements GMP and QMS Training

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.

FDA expects all companies that manufacture, package or hold dietary supplement products to follow 21 CFR 111, the Dietary Supplement current Good Manufacturing Practices (cGMPs).

This training covers the documentation needed for a robust quality management system (QMS) when manufacturing dietary supplements, as well as the best practices to follow when conducting internal audits.

This dietary supplements 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 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.

Supplier or vendor qualification is a crucial component in compliance to 21 CFR 111. The FDA requires that manufacturers of dietary supplements must “qualify” each of their vendors but do not provide guidance on how a company is to perform this qualification.

Supplier or vendor qualification is a crucial component in compliance to 21 CFR 111.

Join us for an interactive, hands-on training designed to provide you with practical tips to help improve efficiency in your master manufacturing record (MMR) and batch production record (BPR) processes.

Dietary supplement manufacturers may be exempt from the preventative control’s requirements of 21 CFR 117, but they are not completely exempt from all aspects of this new regulation.

Food defense is a new area of compliance for the food industry and includes dietary supplement manufacturers.

Dietary supplement manufacturers and raw material suppliers are not exempt from all the requirements of 21 CFR 117 and may be required to have a written food safety plan.

The recent rule changes associated with the Food Safety Modernization Act (FSMA) will have a dramatic impact on the food safety and regulatory landscape for facilities producing products regulated by the FDA, and compliance deadlines for FSMA are quickly approaching.

Dietary supplement manufacturers and raw material suppliers are not exempt from all the requirements of 21 CFR 117 and may be required to have a written supply chain plan.

New regulations for the Foreign Supplier Verification Program (FSVP) have modified requirements for dietary supplement companies and raw material suppliers to be compliant under 21 CFR 1 Subpart L.

The FDA's 21 CFR 111 is a performance-based regulation for the dietary supplement industry.

This convenient instructor-led training focuses on equipment cleaning of dietary supplement facilities in accordance with 21 CFR 111.

This convenient instructor-led training focuses on general cleaning of dietary supplement facilities in accordance with 21 CFR 111.

If you’re entering the nutritional supplement market as a start-up, this training on facility design for Good Manufacturing Practice (GMP) compliance will teach you how to create a facility that complies with industry standards and regulatory requirements.

Are you entering the nutritional supplement market as a startup? This instructor-led course focuses on the steps you need to take for product development and planning for regulatory compliance.

Preparing for an FDA inspection for dietary supplements will help you avoid getting a warning letter and the regulatory and business consequences that come with it.

Manufacturing dietary supplements can be challenging for natural product producers.

In this training, we will address non-conformance report (NCR), CAPA and problem report (PR) writing.

This self-paced course provides a comprehensive overview of 21 CFR 111 - Current Good Manufacturing Practices (cGMPs) for Dietary Supplements.

This self-paced course provides a brief historical review of regulations in the dietary supplement industry and their evolution as key incidents exposed health and safety risks to the consumer.

This self-paced course provides specific guidance on protecting dietary supplement products from contamination and adulteration during the manufacturing process.

This self-paced course covers the requirements for specifications and guidance to establish them, which must be in place to ensure compliance with 21 CFR 111.

This self-paced course covers the requirements for dietary supplement packaging and labeling systems, applicable even if these are the only operations at your facility.

In this 1-hour course, we will discuss the latest trends in FDA observations during their inspections of dietary supplement manufacturers.

This course provides a basic understanding of cleaning and sanitation for dietary supplement facilities.

This course is part of maintaining required compliance to 21 CFR 111 and provides opportunities for ongoing GMP training.

This course will help you understand the basics of auditing and how to conduct an internal audit focused on cGMP and other U.S. FDA requirements.

NSF’s training courses give you the knowledge to ensure that your nutritional supplements and personal care products are compliant with relevant market regulations for labeling and claims. Specialized courses also provide an overview of the NDI and GRAS process to ensure the safety of your ingredients, as well as offer support in determining the authenticity and quality of your botanical ingredients.