With ST&T Research Intl acting as your FDA official correspondent, we will be responsible for the annual registration of the establishment and the device listing. ST&T will be also available to assist you with the labeling and Medical Devices Master Files.
FDA post-market reporting system for use by manufacturers, packers, and distributors of cosmetic products that are in commercial distribution in the United States.
California Safe Cosmetic Program
The US FDA & CUSTOMS (and most other importing countries) require that any domestic or foreign manufacturer and/or distributor who ships into/out of the country must have a local agent who can respond to FDA NDC filing/reporting, and Customs, legal and regulatory matters or questions which may arise concerning their products. ST&T has specialists who provide clients with these Regulatory Agent Services.
Acting as your U.S. Agent, your Company will be provided legal & science support for its efforts to market products in the USA.