This one-hour webinar provides an overview of FDA regulatory enforcement actions. You will learn about FDA regulations and laws pertaining to over-the-counter (OTC) drugs and cosmetics marketed in the United States. The presentation will discuss real scenarios, including labeling dos and don’ts. The objective of the webinar is to teach manufacturers, importers, and the like, how to navigate FDA’s regulatory framework, provide TOP compliance tips to avoid FDA enforcement actions, and strategies when you are faced with an enforcement action.

In This Webinar You Will Learn:
– How FDA Regulates OTC Drug and Cosmetic Products (and How to Differentiate Your Product)
– Labeling Dos and Don’ts (Including a Discussion on Intended use)
– Top Tips for Compliance
– Types of FDA Enforcement Actions
– Best Practices for Responding to Enforcement Actions (Including Real Life Examples)

– Jennifer Diaz
– Denise Calle

Who Should Attend:
– Importers
– Customs Brokers
– Regulatory Affairs Professionals
– In-house Legal Counsel
– Product Development Managers
– Others Interested in FDA

Eligible for 1 CCS/MCS/CES/MES NEI Credit
– Input your NCBFAA NEI ID number at the time of registration to receive credit