Navigating Dietary Supplement Regulations: From Compliance to Competitive Advantage
Master FDA Compliance in the Age of CBD and Personalized Nutrition!
Instructor :
Meredith Crabtree
Webinar ID:
10693
Date: DEC 30, 2024 (MON)
Start Time: 10 AM PT - 11:30 AM PT
Duration: 90 Mins.
What you will learn
- Define And Explore Dietary Supplements’ Types And Purposes
- Unpack FDA’s Role And Authority In Supplement Regulation
- Detail DSHEA’s Impact And FDA’s Regulatory Scope
- Master Labeling, Claims, And GMPs For Compliance
- Navigate FDA’s Post-Market Surveillance And …
-
- Define And Explore Dietary Supplements’ Types And Purposes
- Unpack FDA’s Role And Authority In Supplement Regulation
- Detail DSHEA’s Impact And FDA’s Regulatory Scope
- Master Labeling, Claims, And GMPs For Compliance
- Navigate FDA’s Post-Market Surveillance And Adverse Event Processes
- Address Challenges Like Mislabeling And Adulteration Concerns
- Discuss Emerging Trends Like CBD And Personalized Nutrition
Course Description
-
- How confident are you in your understanding of the FDA’s dietary supplement oversight?
- Are you up-to-date with the Dietary Supplement Health and Education Act and its implications?
- What unforeseen challenges might you be overlooking?
“Navigating Dietary Supplement Regulations: From Compliance to Competitive Advantage” is a 1.5-hour intensive webinar designed to deepen participants’ understanding of the FDA’s regulatory role over dietary supplements.
“ Participants will learn about critical labeling requirements, adverse event reporting, and emerging trends like CBD and personalized nutrition.“
This session will:
-
- Clarify the functions and benefits of dietary supplements.
- Illuminate the FDA’s authoritative scope and responsibilities within the industry.
- Discuss critical regulatory requirements.
- Address emerging challenges and issues that affect the sector.
Key Learning Outcomes:
-
- Understanding the Essentials: Gain a solid grasp of the various dietary supplements available, their benefits, and potential risks, while debunking common misconceptions.
- Navigating Regulations: Learn about the impact of the Dietary Supplement Health and Education Act (DSHEA) and the FDA’s regulatory framework including labeling, claims requirements, and GMPs for manufacturing.
- Enhancing Safety and Compliance: Explore the FDA’s mechanisms for post-market surveillance and adverse event reporting.
- Identifying Challenges: Discuss significant issues like product safety, mislabeling, adulteration, and deceptive marketing practices, with a focus on the repercussions of contaminated or adulterated supplements.
- Looking Forward: Engage in dialogue on future trends and the evolving landscape of dietary supplement regulation, including topics like CBD, hemp-derived products, novel ingredients, and personalized nutrition.
Participants will emerge from the training equipped to make informed decisions, either as consumers or industry stakeholders, through a heightened awareness of the complexities of dietary supplement regulation and ongoing regulatory updates.
Join Now!
-
- How confident are you in your understanding of the FDA’s dietary supplement oversight?
- Are you up-to-date with the Dietary Supplement Health and Education Act and its implications?
- What unforeseen challenges might you be overlooking?
“Navigating Dietary Supplement Regulations: From Compliance to Competitive Advantage” is a 1.5-hour intensive webinar designed to deepen participants’ understanding of the FDA’s regulatory role over dietary supplements.
“ Participants will learn about critical labeling requirements, adverse event reporting, and emerging trends like CBD and personalized nutrition.“
This session will:
-
- Clarify the functions and benefits of dietary supplements.
- Illuminate the FDA’s authoritative scope and responsibilities within the industry.
- Discuss critical regulatory requirements.
- Address emerging challenges and issues that affect the sector.
Key Learning Outcomes:
-
- Understanding the Essentials: Gain a solid grasp of the various dietary supplements available, their benefits, and potential risks, while debunking common misconceptions.
- Navigating Regulations: Learn about the impact of the Dietary Supplement Health and Education Act (DSHEA) and the FDA’s regulatory framework including labeling, claims requirements, and GMPs for manufacturing.
- Enhancing Safety and Compliance: Explore the FDA’s mechanisms for post-market surveillance and adverse event reporting.
- Identifying Challenges: Discuss significant issues like product safety, mislabeling, adulteration, and deceptive marketing practices, with a focus on the repercussions of contaminated or adulterated supplements.
- Looking Forward: Engage in dialogue on future trends and the evolving landscape of dietary supplement regulation, including topics like CBD, hemp-derived products, novel ingredients, and personalized nutrition.
Participants will emerge from the training equipped to make informed decisions, either as consumers or industry stakeholders, through a heightened awareness of the complexities of dietary supplement regulation and ongoing regulatory updates.
Join Now!
Why you should attend
The stakes are high as the FDA intensifies its focus on safety and marketing practices. Is your team ready to face these growing challenges with confidence?
Attending this webinar offers invaluable insights into the complex regulatory landscape of the FDA’s oversight of dietary supplements.
“ You’ll gain insights into new regulations, effective compliance strategies, and proactive measures to safeguard your products and enhance market credibility.“
This training is vital for anyone involved in the industry—from manufacturers and marketers to healthcare professionals and consumers—providing them with the knowledge needed to navigate confidently and make informed decisions.
Key Benefits:
-
- Deep Regulatory Insight: Understand the FDA’s extensive authority and responsibilities, illuminating the regulatory framework that governs dietary supplements.
- Compliance Mastery: Dive into essential compliance aspects including labeling, claims, and manufacturing practices. Grasping these elements is crucial for avoiding non-compliance penalties, product recalls, or legal issues.
- Enhancing Safety and Quality: Learn about the FDA’s regulations on product testing, ingredient sourcing, and manufacturing practices that prioritize consumer safety and produce high-quality supplements.
- Risk Mitigation Strategies: Gain insights into proactive strategies to identify and mitigate risks like mislabeling, adulteration, and deceptive marketing practices, protecting both consumers and the industry’s integrity.
- Emerging Trends and Issues: Explore evolving issues such as the regulation of CBD and hemp-derived products, novel ingredients, and personalized nutrition, staying informed for better decision-making.
- Consumer Empowerment: Equip yourself with the knowledge to discern reliable products, understand potential risks, and make educated choices about supplement usage.
This webinar is designed not only to educate but also to empower participants, ensuring they are well-prepared to adapt to an ever-evolving regulatory and market landscape.
Enroll Now!
The stakes are high as the FDA intensifies its focus on safety and marketing practices. Is your team ready to face these growing challenges with confidence?
Attending this webinar offers invaluable insights into the complex regulatory landscape of the FDA’s oversight of dietary supplements.
“ You’ll gain insights into new regulations, effective compliance strategies, and proactive measures to safeguard your products and enhance market credibility.“
This training is vital for anyone involved in the industry—from manufacturers and marketers to healthcare professionals and consumers—providing them with the knowledge needed to navigate confidently and make informed decisions.
Key Benefits:
-
- Deep Regulatory Insight: Understand the FDA’s extensive authority and responsibilities, illuminating the regulatory framework that governs dietary supplements.
- Compliance Mastery: Dive into essential compliance aspects including labeling, claims, and manufacturing practices. Grasping these elements is crucial for avoiding non-compliance penalties, product recalls, or legal issues.
- Enhancing Safety and Quality: Learn about the FDA’s regulations on product testing, ingredient sourcing, and manufacturing practices that prioritize consumer safety and produce high-quality supplements.
- Risk Mitigation Strategies: Gain insights into proactive strategies to identify and mitigate risks like mislabeling, adulteration, and deceptive marketing practices, protecting both consumers and the industry’s integrity.
- Emerging Trends and Issues: Explore evolving issues such as the regulation of CBD and hemp-derived products, novel ingredients, and personalized nutrition, staying informed for better decision-making.
- Consumer Empowerment: Equip yourself with the knowledge to discern reliable products, understand potential risks, and make educated choices about supplement usage.
This webinar is designed not only to educate but also to empower participants, ensuring they are well-prepared to adapt to an ever-evolving regulatory and market landscape.
Enroll Now!
Course Agenda
Looking for a customized version of this training tailored specifically to your team’s needs and delivered at your convenience?
-
- Contact us at support@compliancemeet.com to explore your options!
- We offer tailored sessions that focus on your specific areas of interest, available online or in-person to fit your schedule.
Understanding Dietary Supplements
-
- Definition and Purpose: Clarify what dietary supplements are and their intended uses.
- Types: Explore the various types of dietary supplements available.
- Benefits and Risks: Discuss the benefits and potential risks associated with dietary supplement usage.
- Common Misconceptions and Challenges: Address widespread misunderstandings and obstacles within the industry.
The Role of the FDA
-
- Introduction: Overview of the Food and Drug Administration (FDA).
- Regulatory Authority: Examine the FDA’s authority in regulating dietary supplements.
- DSHEA Overview: Discuss the impact of the Dietary Supplement Health and Education Act (DSHEA).
- Responsibilities and Limitations: Outline the FDA’s duties and constraints in overseeing the industry.
FDA Regulations and Requirements for Dietary Supplements
-
- Labeling and Claims: Review labeling and claims requirements for dietary supplements.
- NDI Notification Process: Explain the New Dietary Ingredient (NDI) notification process.
- GMPs: Highlight Good Manufacturing Practices (GMPs) for dietary supplement manufacturers.
- Ensuring Product Quality and Safety: Emphasize the importance of maintaining high-quality and safe products.
Post-Market Surveillance and Adverse Event Reporting
-
- Surveillance System: Describe the FDA’s post-market surveillance system for dietary supplements.
- Adverse Event Reporting: Detail the requirements and processes for adverse event reporting.
- FDA’s Response: Discuss the FDA’s actions in response to reported adverse events.
Challenges and Concerns in Dietary Supplement Oversight
-
- Safety and Regulatory Challenges: Highlight product safety concerns and regulatory challenges.
- Mislabeling, Adulteration, and Deceptive Practices: Explore issues related to mislabeling, adulteration, and deceptive marketing.
- Implications of Contamination: Discuss the implications of contaminated or adulterated supplements.
Emerging Issues and Future Developments
-
- Current Trends: Examine current trends and developments in dietary supplement regulation.
- CBD and Hemp Products: Discuss regulation surrounding CBD and hemp-derived products.
- Novel Ingredients and Personalized Nutrition: Consider novel ingredients and the rise of personalized nutrition.
- Regulatory Updates: Stress the importance of staying updated with regulatory changes.
Promoting Consumer Awareness
-
- Education Importance: Underscore the importance of consumer education in making informed decisions.
- Identifying Reliable Products: Provide tips on identifying reliable products and recognizing potential risks.
- Navigating the Market: Offer strategies for effectively navigating the dietary supplement market.
BONUS:
-
- PDF copy of the presentation handout for your future reference.
- Soft copy of the certificate of completion on request.
- Q&A Session with the Presenter: Get your pressing questions answered verbally, via chat or email
Looking for a customized version of this training tailored specifically to your team’s needs and delivered at your convenience?
-
- Contact us at support@compliancemeet.com to explore your options!
- We offer tailored sessions that focus on your specific areas of interest, available online or in-person to fit your schedule.
Understanding Dietary Supplements
-
- Definition and Purpose: Clarify what dietary supplements are and their intended uses.
- Types: Explore the various types of dietary supplements available.
- Benefits and Risks: Discuss the benefits and potential risks associated with dietary supplement usage.
- Common Misconceptions and Challenges: Address widespread misunderstandings and obstacles within the industry.
The Role of the FDA
-
- Introduction: Overview of the Food and Drug Administration (FDA).
- Regulatory Authority: Examine the FDA’s authority in regulating dietary supplements.
- DSHEA Overview: Discuss the impact of the Dietary Supplement Health and Education Act (DSHEA).
- Responsibilities and Limitations: Outline the FDA’s duties and constraints in overseeing the industry.
FDA Regulations and Requirements for Dietary Supplements
-
- Labeling and Claims: Review labeling and claims requirements for dietary supplements.
- NDI Notification Process: Explain the New Dietary Ingredient (NDI) notification process.
- GMPs: Highlight Good Manufacturing Practices (GMPs) for dietary supplement manufacturers.
- Ensuring Product Quality and Safety: Emphasize the importance of maintaining high-quality and safe products.
Post-Market Surveillance and Adverse Event Reporting
-
- Surveillance System: Describe the FDA’s post-market surveillance system for dietary supplements.
- Adverse Event Reporting: Detail the requirements and processes for adverse event reporting.
- FDA’s Response: Discuss the FDA’s actions in response to reported adverse events.
Challenges and Concerns in Dietary Supplement Oversight
-
- Safety and Regulatory Challenges: Highlight product safety concerns and regulatory challenges.
- Mislabeling, Adulteration, and Deceptive Practices: Explore issues related to mislabeling, adulteration, and deceptive marketing.
- Implications of Contamination: Discuss the implications of contaminated or adulterated supplements.
Emerging Issues and Future Developments
-
- Current Trends: Examine current trends and developments in dietary supplement regulation.
- CBD and Hemp Products: Discuss regulation surrounding CBD and hemp-derived products.
- Novel Ingredients and Personalized Nutrition: Consider novel ingredients and the rise of personalized nutrition.
- Regulatory Updates: Stress the importance of staying updated with regulatory changes.
Promoting Consumer Awareness
-
- Education Importance: Underscore the importance of consumer education in making informed decisions.
- Identifying Reliable Products: Provide tips on identifying reliable products and recognizing potential risks.
- Navigating the Market: Offer strategies for effectively navigating the dietary supplement market.
BONUS:
-
- PDF copy of the presentation handout for your future reference.
- Soft copy of the certificate of completion on request.
- Q&A Session with the Presenter: Get your pressing questions answered verbally, via chat or email
Who is this course for
Maximize the Learning Experience in A Group Setting!
-
- Quality Assurance and Quality Control Personnel
- Regulatory Affairs Professionals
- Compliance Officers
- Product Development and Formulation Scientists
- Marketing and Sales Professionals in the Dietary Supplement Industry
- Consumer Advocacy Groups or Organizations Interested in Dietary Supplement Regulation
- Health and Wellness Coaches
- Educators or Instructors in the field of Nutrition and Supplements
Maximize the Learning Experience in A Group Setting!
-
- Quality Assurance and Quality Control Personnel
- Regulatory Affairs Professionals
- Compliance Officers
- Product Development and Formulation Scientists
- Marketing and Sales Professionals in the Dietary Supplement Industry
- Consumer Advocacy Groups or Organizations Interested in Dietary Supplement Regulation
- Health and Wellness Coaches
- Educators or Instructors in the field of Nutrition and Supplements
Instructor Profile
Meredith L. Crabtree has over 30 years’ experience in regulated industries, ranging from Blood, Plasma, Tissue, Laboratory, Pharma, Medical Device, Cosmetics, Supplements, and Animal Health. This includes manufacturing, packaging, labelling and distribution operations. Meredith is the owner of MLKC Consulting is s a Quality Consultant specializing in product label reviews, 3rd party inspections, Consent Decree and Recall support. She also performs regulatory assessments and Quality trainings.
