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The FDA and Dietary Supplement Oversight - What does that mean?" is a comprehensive training session designed to provide participants with an understanding of the role of the Food and Drug Administration (FDA) in regulating dietary supplements. The training aims to clarify the purpose and benefits of dietary supplements, highlight the FDA's authority and responsibilities in overseeing the industry, discuss regulatory requirements, and address emerging issues and challenges.
The training will emphasize the importance of dietary supplements and the need for effective oversight. Participants will gain insights into the different types of dietary supplements available in the market, their benefits, and potential risks. Common misconceptions and challenges in the industry will also be addressed.
The session then dives into the role of the FDA in regulating dietary supplements. Participants will learn about the FDA's authority and the impact of the Dietary Supplement Health and Education Act (DSHEA) on supplement regulation. The training explores the FDA's regulatory framework, including labeling and claims requirements, the New Dietary Ingredient (NDI) notification process, and good manufacturing practices (GMPs) for dietary supplement manufacturers. The FDA's post-market surveillance and adverse event reporting system will also be discussed.
Challenges and concerns in dietary supplement oversight will be explored, including product safety, mislabeling, adulteration, and deceptive marketing practices. The implications of contaminated or adulterated supplements will be highlighted, underscoring the importance of consumer awareness and education in mitigating risks.
The training will have a discussion on future developments and emerging issues in dietary supplement regulation. Participants will explore ongoing efforts to strengthen the FDA's oversight of the industry and examine emerging topics such as CBD and hemp-derived products, novel ingredients, and personalized nutrition. The importance of staying informed about regulatory updates and changes will be emphasized.
Overall, this training aims to equip participants with the knowledge and awareness necessary to navigate the complex landscape of dietary supplement regulation and make informed decisions as consumers or industry stakeholders.
In summary, attending this training offers the opportunity to gain a comprehensive understanding of the FDA's role in dietary supplement oversight, comply with regulatory requirements, prioritize product safety, mitigate risks, stay informed about emerging issues, empower consumers, and engage in ongoing professional development
Meredith Crabtree has over 25 years’ experience in regulated industries ranging from Pharma, Medical Device, Biologics, Laboratory testing, Cosmetics, and Supplements. She has worked in both manufacturing and distribution as well as Human Health and Animal Health. Meredith currently works as a Quality Consultant performing label reviews, 3rd party inspections, Consent Decree and Recall support. She also performs regulatory assessments and Quality training. Meredith has a degree in Medical Technology and is currently obtaining a degree in Quality Systems.