| http://www.w3.org/ns/prov#value | - Companies interested in introducing a new drug into the US market in most cases must submit a New Drug Application (NDA) to the FDA, which must include extensive information and data on the drug???s safety and effectiveness, such as the drug???s chemistry, manufacture, animal and in vitro studies, clinical data, and the like.[58] Drugs developed through genetic engineering must go through the same
|
