Larisa Pavlick has nearly 30 years of combined experience from industry – spanning dietary supplement regulatory, quality and product development. She spent nearly eight years at the U.S. Food and Drug Administration (FDA) as an investigator (dietary supplement, food safety, GMP [good manufacturing practice]), followed by almost eight years working with two different trade associations representing dietary supplements, natural products and consumer health care goods for self-care.  

Larisa has seen the industry from all angles and dedicates her time and energy to share these experiences with others. Her favorite (and frequent) feedback has been her ability to simplify regulations and FDA guidance. Pavlick has been told she has the unique gift of putting “regulatory speak” into simple language with actionable steps to help organizations improve their quality systems and compliance.