Flavine provides support to the manufacturers it represents as well as to its customers in all areas of regulatory affairs requirements with its own experienced in-house staff in the USA, Germany and China. Flavine also engages outside regulatory affairs consultants for plant audit, DMF/CoS preparation and FDA/GMP inspections when necessary to expedite the approval process. Flavine's manufacturers have an excellent track record for prompt DMF preparation, filing and successful FDA inspections.

Flavine continues to add value after approval by providing integrated sourcing, logistics, import and distribution services, for the benefit of both the API manufacturer and Flavine's customers. These same services have also allowed Flavine to establish strong positions in products not requiring the same level of regulatory approval, such as Nutritional Supplements and Phyto-Pharmaceuticals and APIs which are for OTC applications.