In this session, you will learn the Big 5 and solutions to reduce the risk of regulatory problems in product design, manufacturing, labeling, and marketing your dietary supplements, OTC drugs, cosmetics, and homeopathic products. You will learn some high-level methods to minimize your risks with these (and potentially other) highly-regulated consumer products. With time, we will get into the woes of product litigation and importing risks.
About Benjamin L. England
Mr. England is the CEO and Founder of Benjamin L. England & Associates, LLC and FDAImports.com, LLC. He routinely represents domestic and foreign companies of all sizes, assisting them in identifying FDA, USDA, FTC, EPA, and state requirements. His representation enables his clients to better understand and fully comply with federal and state requirements and reduce the risk of regulatory interference with products being imported, exported, or distributed in interstate commerce.
A 17-year veteran of FDA, Mr. England served as the Regulatory Counsel to the Associate Commissioner for Regulatory Affairs. Before this, he served in scientific, inspectional, compliance, criminal, and civil enforcement capacities as an FDA Consumer Safety Officer, Compliance Officer, a Senior Special Agent with FDA’s Office of Criminal Investigations (OCI), and an analytical regulatory microbiologist.