U.S.A. FDA medicines manage the introduction

U.S.A. FDA medicines manage the introduction
FDA whether the intersection of American and the intersection of food and medicine manage English abbreviation of administration, the English full name should be Food and Drug Administration. It is authorized by the US Congress namely federal government, specially supreme law enforcement agency engaged in food and medicines management. FDA is one by the doctor, lawyer, little biologists, what professional personages such as the pharmacologist, chemist and statistician,etc. make up is devoted to protecting, promoting and improving the control mechanism that American people's healthy hygiene of government controls. FDA must guarantee all food, medicines, cosmetics and medical apparatus are safe and effective to the human body on the American market. U.S.A. FDA nearly has 10,000 formal staff, 2100 among them are scientists with a degree, include 900 chemists and 300 little biologists. They work in about 40 laboratories, 100 kinds of new medicines are listed. FDA controls the value made, imported, transported, stored and sold of the products and is up to 1,000 billion dollars every year, it is equivalent to 1/4 of the consumption every year of American people. FDA has 1100 inspectors with license, about more than 95000 companies in U.S.A. which they supervised. Among them 15000 companies are spotted check by the FDA every year. So as to ensure it is correct that the production process of the products of these producers accords with the regulation of FDA and label of the products. With the enhancement of people's health care consciousness, and the old age day by day of American society, the demands for the medicine curing old age and chronic disease of people are increasing constantly, in order to improve the national health level, the medical demand for plant medicine of consumer goods market of U.S.A. of expenses which reduces medicine increases rapidly. In order to promote the development of medicine industry of the natural plant, US Congress and FDA issued " health education bill of nutritive food " in 1994 (DSHEA) ,Stipulate clearly plant medicine can be regarded as the nutritive food and circulated, but does not need to be approved by FDA. Recently, FDA make " plant medicine study the guide " again ,To plant medicine (traditional Chinese medicine) Apply for FDA and sanction proposing special management as new medicine, and estimate that can issue in the near future formally. Development in U.S.A. of medicine industry of traditional plant of promotion that U.S.A. FDA new standardard management and fashion are with big demand. Since 1994, every annual mean of market of American plant medicine is increased progressively with 25% rate, at present, the market always sells and already reaches 2,200 million dollars; One of the main health insurance management organizations of U.S.A. - --Oxford insures, already plant medicine (including Chinese medicine, traditional Chinese medicine) List the category in submitting an expense account; Several biggest pharmacy enterprises in the world, have all already entered the medicine consumer goods market of plant in succession; The company specializing in traditional plant medicine and developing increases rapidly too, the medicine industrial development of the traditional plant has already entered one new historical time in U.S.A.. Person the intersection of strength and compound root of red-rooted salvia drip pill as treat the intersection of heart and the intersection of brain and vascular natural the intersection of plant and medicine of disease day, take the lead in through the strict examination of U.S.A. FDAIND in the capacity of medicines, this has far-reaching influence on pushing plant rapid development, also entered world medicines market to Chinese medicine of our countrying brings the opportunity.

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