PHAR 303 Lecture Notes - Lecture 6: Toxics Release Inventory, Canadian Environmental Protection Act, 1999, Veterinary Medicine
30 Jan 2016
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Document Summary
Trying to figure out the basis or substantiate the kind of associations described in epidemiological studies. We"re trying to characterize the toxicity profiles of chemicals (or biologicals) All drugs (developed for human use) are tested: o o. Data are reviewed by regulatory agencies prior to the approval of clinical. Preclinical toxicology trials (first administration to humans) o o. Food and drug administration (fda) for the us. The ich is the international conference on harmonisation of technical. Requirements for registration of pharmaceuticals for human use (ich) It is unique in bringing together the regulatory authorities and pharmaceutical industry of europe, japan and the us to discuss scientific and technical aspects of drug registration. We need to know about the chemicals that are released from new industries. There are different kinds of regulatory processes available for all the types of chemicals used compared to what is made for human use.
