Expert Jaclyn Bellomo will take you through an introduction to the FDA’s expanded authority and regulatory power concerning Adverse Events in cosmetics. This new requirement will significantly impact how companies handle health-related consumer reports, as the FDA can request records if there is a reasonable probability of causing a serious adverse health consequence or public health concern. More importantly, companies need to be prepared for upcoming FDA inspections where they will be asked to provide proper records. FDA’s new authority allows for Mandatory Recalls and Facility Suspensions posing serious risks to cosmetic brands.
- Understanding new Adverse Event Requirements for Cosmetics
- Requirements for receiving adverse events and upcoming deadline for cosmetic labels
- Process and tips for implementation of an Adverse Event intake system
- Adverse Event Management Software Demonstration
