Cosmetic Facilities
The FD&C Act prohibits the marketing of adulterated or misbranded cosmetics in interstate commerce. Violations of the Act involving product composition--whether they result from ingredients, contaminants, processing, packaging, or shipping and handling--cause cosmetics to be adulterated and subject to regulatory action. VTI can help you ensure that your processes, facilities, equipment and procedures adhere to GMP requirements (21 CFR parts FD&C) and are validated according to regulatory (FDA) standards.