Producing controlled APIs for manufacturers of ethical pharmaceutical products requires a world-class regulatory compliance management system, a series of licenses governing the handling and transportation of narcotics, and a thorough understanding of country-by-country restrictions pertaining to the import and export of APIs and finished dosage forms (FDFs).
Noramco has a 40+ year exemplary track record of success managing narcotic raw materials and controlled APIs in accordance with international rules and country-by-country regulations.
A global operation with a global workforce, Noramco offers pharmaceutical product makers the assurance of regulatory compliant processes worldwide, the benefits of fully-trained personnel, and the integrity of products produced at fully registered cGMP production sites located in Western Europe, and in the United States, including Delaware.
With Noramco, you can work with a company that holds exemplary FDA, EDQM, and DEA compliance records for controlled substances, from schedule I to schedule III.
