On August 31, 2014, after 5 days of checking, TERI pharmaceutical company limited the production of tartaric acid in Ningxia tylosin tylosin tartrate powder, pigment granules formally approved United States drug license. United States pharmaceutical license is known as the world’s most stringent quality standards for pharmaceutical production. United States FDA certified drugs enter the United States market on the “stepping stone”, TERI pharmaceuticals also takes this opportunity to open up United States and global market development and branding.
United States food and Drug Administration (FDA) is the world’s food and drug industry’s most authoritative official bodies. FDA certification is widely regarded as the world’s most stringent quality standards for pharmaceutical production. Get FDA certification means to enter the United States market opportunities, but also the pharmaceutical enterprise products to enter the European and American market a “major pass”. In a 5 day period, FDA-certified professionals on this Terry Gross on pharmaceutical quality system, production system, materials, systems, equipment and facility systems, packaging labelling system, file system, such as a rigorous site inspection, facility one by one. Certified experts gave TERI pharmaceutical high recognition and good evaluation and eventually pass the inspection to assess.
