The US FDA and Dietary Supplement Oversight" explores the crucial role of the U.S. Food and Drug Administration (FDA) in regulating the rapidly growing dietary supplement industry. This training provides a deep understanding of FDA oversight, challenges faced, and key regulations.
The dietary supplement industry, comprising vitamins, minerals, herbs, and more, presents unique regulatory challenges separate from drugs. The training introduces participants to supplement types, FDA responsibilities, and regulations for safety and accurate labeling.
The FDA oversees the industry by establishing guidelines, monitoring safety, and enforcing regulations against deceptive marketing. The training delves into challenges, such as the absence of pre-market approval and limited FDA resources impacting comprehensive regulation. Adverse event reporting and monitoring are highlighted for strengthening oversight.
The focus shifts to regulations, emphasizing the Dietary Supplement Health and Education Act (DSHEA) of 1994, Good Manufacturing Practices (cGMP), and the New Dietary Ingredient (NDI) notification process. Safety considerations, including ingredient safety assessments, risks, contamination, and interactions with medications, are explored to ensure transparency and informed choices.
Labeling and advertising requirements are crucial for consumer understanding. The training covers nutrition facts, claims, disclaimers, and ingredient lists. Enforcement actions by the FDA, including inspections, warning letters, recalls, and potential legal consequences for non-compliance, are discussed to emphasize the importance of compliance programs.
The training concludes by highlighting reliable information sources, such as the FDA's website and guidance documents. Participants are encouraged to use authoritative resources and understand the role of healthcare professionals in providing accurate information for informed decision-making.
In summary, "The US FDA and Dietary Supplement Oversight" equips participants with comprehensive knowledge of the FDA's role, industry challenges, and regulatory compliance, ensuring they can navigate the complex dietary supplement landscape and contribute to consumer safety and transparency.
Stay on top of the rules and keep people safe in the growing dietary supplement industry. Learn all about how the FDA looks after these supplements and what rules they follow. This training will give you the know-how and tools to understand how supplements are regulated, avoid risks, and follow the rules. Don't let false claims, harmful substances, or rule-breaking harm your reputation or people's health. Join us to stay in the loop, protect your business, and make smart choices in the changing world of supplement regulations.
Stay on top of the rules and keep people safe in the growing dietary supplement industry. Learn all about how the FDA looks after these supplements and what rules they follow. This training will give you the know-how and tools to understand how supplements are regulated, avoid risks, and follow the rules. Don't let false claims, harmful substances, or rule-breaking harm your reputation or people's health. Join us to stay in the loop, protect your business, and make smart choices in the changing world of supplement regulations.
Meredith Crabtree
Meredith Crabtree has over 25 years’ experience in regulated industries, ranging from Blood, Plasma, Tissue, Laboratory, Pharma, Medical devices, Cosmetics, Supplements, and Animal Health manufacturing and distribution. Meredith 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.
Maximizing Productivity with ChatGPT: AI Solutions for HR, …
Excel - Pivot Tables - The Key To Modern Data Analysis and …
New EEOC Report: Workplace Harassment Prevention Not Workin…
Human Error Reduction Techniques for Floor Supervisors
21 CFR Part 11 - Compliance for Electronic Records and Sign…
Form W-9 Compliance to Avoid Penalties: TIN Verification, B…
Transforming Change and Conflict into Diverse-Inclusive-Col…
Re-imagine Finance & Accounting Made Simple. Three Webinars…
Navigating 2025 Employment Laws: What Every Employer Needs …
Managing Difficult Employee Conversations
ChatGPT and Project Management: Leveraging AI for Project M…
Future Of Forecasting And Budgeting With Rolling Forecast
Handbook Overhaul 2026: Compliance, OBBB Act & Beyond
Internal Controls in Accounts Payable
The FMLA - An Employer's Guide to Compliance and Employee A…
Excel Power Skills: Master Functions, Formulas, and Macros …
Develop People Intelligence: Is Your Communication Style as…
The Impact of Artificial Intelligence on Your Workforce
AI in Everyday Work – help with Microsoft products
How to Document Employee Discussions and Why it is Important
Construction Lending And Real Credit Administration: Evalua…
The Anti-Kickback Statute: Enforcement and Recent Updates
Navigating FDA Inspections: From SOP to 483
2025 EEOC & Employers: Investigating Claims of Harassment …
2-Hour Virtual Seminar on DeepSeek R1 for Business and Mark…
Risk Analysis in the Medical Device Design Process
Introduction to Microsoft Power BI Dashboards
How To Get Control of Your Day, Life & Career - Time Manage…
AI Across the Business: Practical Use Cases for Founders an…
6-Hour Virtual Seminar on Learning the Highlights of Excel …
Female to Female Hostility @Workplace: All you Need to Know
Writing Effective 483 and Warning Letter Responses
FDA Recommendations for Artificial Intelligence/Machine Lea…
Language is Code - Intro to AI - Generative AI - ChatGPT an…
Understanding EBITDA – Definition, Formula & Calculation