A nutraceutical product with quality as good as a pharmaceutical drug is possible when you apply the required GMP norms. Technological feasibility, safety, and cost efficiency are a few things to take into consideration when applying these GMP principles. This dietary supplement formulation training covers various instrumental topics to understand critical regulations.
If you are looking for training that is way beyond content-draining and one-sided seminars, this dietary supplement course is perfect for you. Whether you are a business owner or a manufacturing unit director, warning letters and injunctions are the last things you would wish for.
Get enrolled in this course and absorb all the useful insights related to the industry!
Course Overview
The main problem arises when manufacturers, distributors, and consumers don’t understand the efficacy of dietary supplements. Due to a boom in the market, producers are coming up with supplements that are deficient.
Additionally, the ease of access and over-the-counter availability have diluted the importance of dietary supplements. This course is here to change the narrative and bridge the existing gaps.
Dietary supplement formulation training gives a comprehensive introduction to programming the entire manufacturing unit. Moreover, you will get to know the possible issues you might face while testing the products.
Here are some benefits of taking a course on regulatory compliance for dietary supplements:
- Understanding FDA expectations
- Knowing the rules and regulations to follow during the audits
- Improving the GMPs to upgrade operations in the unit
- Fundamentals of physical and chemical properties of the ingredients
- Stability studies and categorization
- Techniques to create a formulation that passes multiple checkpoints.
Course Content
The detailed seminar is divided into two days and the first day consists of dietary supplements regulation in the US. As a result, the session will cover the following topics:
Course Provider
Travis Austin MacKay,
Plexus WorldwideTravis MacKay is the Director of Regulatory Affairs for Plexus Worldwide, a leading direct sales company with a range of products dedicated to helping others obtain health and happiness. He currently oversees international regulatory compliance activities driving strategic direction focused on claims development and substantiation strategy, product development and commercialization, international formulation considerations, and quality testing & validation.
Travis has 20 years of quality and regulatory experience, including prior regulatory affairs leadership positions within well-respected, global consumer product companies. He has a passion for mentoring regulatory professionals to develop robust compliance systems that keep business moving forward.
Travis Graduated from the University of Utah in 2002 with a B.S. in Behavioral Science and Health (Human Health Emphasis). He is a fly-fishing enthusiast, a college football fan, an exercise junky, and a lover of classic cars. He escapes the noise by spending time with his family in the outdoors of beautiful Arizona.
Who Should Attend
The course is designed to benefit professionals associated with different departments of dietary supplement manufacturing units, such as:
- Quality testing and assurance: Helps them understand the basic parameters of testing the final product and by-products.
- In-house auditors: Assists them in doing strict audits to avoid product recalls and FDA inspection failures
- Suppliers and distributors: Makes them aware of licensing, marketing, and basic compliance related to dietary supplement distributions.
- Labelling and packaging: Labels play an essential role in maintaining transparency about the ingredients. Hence, one must give the highest priority to the norms associated with labeling and packaging. This course consists of 3 rounds of discussion on this topic.
