Creating and managing an International Sales Network requires skills and experiences in the areas of sales, marketing and export compliance that are not always present in the enterprise’s structure.
For this reason BYM! offers its support to manufacturers acting like an outsourced export trade office being able to retrieve the data and information needed for effective business development in new geographical areas.
U.S. FDA is responsible for protecting the public health by assuring that foods (except for meat from livestock, poultry and some egg products which are regulated by the U.S. Department of Agriculture), electronic products, cosmetics and dietary supplements are safe, wholesome, sanitary and properly labeled; ensuring that human and veterinary drugs, and vaccines and other biological products and medical devices intended for human use are safe and effective.
As established by the DM 21 December 2009 outlining “Modifications and integrations of the decree of the Ministry of Health of 20 February 2007 governing “New conditions for the obligations provided for by Article 13 of the legislative decree of 24 February 1997, n. 46 and subsequent modifications, and for the registration of active implantable devices as well as for the registration in the repertory of medical devices”, all medical devices, placed on Italian market for first time starting from 1 May of 2007, must be register in the database of NSIS of Ministry of Health
The international standard “ISO 22000 Food Safety Management Systems – Requirements for any organization involved in the worldwide food chain supply ” Outlines and defines the standardized requirements for planning and implementing a food safety management system in any company involved in the agro-food and food manufacturing industries.