With a new Congress and ever evolving regulatory priorities and guidance from the Food and Drug Administration (FDA) and the Federal Trade Commission (FTC), 2011 promises to be a watershed year for the dietary supplement industry. Be in the best position to respond to legislative and regulatory changes.
Claudia Lewis-Eng and other industry professionals will discuss important information on the latest developments from Capitol Hill, federal regulators and the states, trends to watch, and what to expect in the coming year. Issues will include FDA inspections and good manufacturing practices of dietary supplement facilities, new dietary ingredients (NDIs), product classifications, claims substantiation, and more.
Registration and more information is available on FDLI's website.