WHAT YOU'LL LEARN 💡

💡Within the intricate web of regulations governing dietary supplements in the United States, a stringent framework prevails, overseen with meticulous care by the Food and Drug Administration (FDA).

At the core of this regulatory framework stands the Dietary Supplement Health and Education Act (DSHEA) of 1994, a foundational pillar that establishes precise guidelines governing the realms of manufacturing, labeling, and marketing.

Compliance is not an option but a mandate for all stakeholders, including manufacturers, distributors, and marketers. Adhering to the exacting standards set forth by the FDA and DSHEA is paramount to success.

During this event, we will delve deeply into the steps required to achieve and maintain compliance, equipping you with the knowledge necessary to navigate the intricate regulatory landscape of dietary supplements in the USA effectively. 

📒 The agenda:

• Regulatory framework in the US
• Labeling of food supplements
• Authorized claims