A bioequivalence study is usually carried out for generic drug product. The study evaluates clinical differences in the bioavailability of two distinct drugs. These studies are conducted to assess the efficacy of a new drug product which may have a few different excipients or inactive ingredients. Bioequivalence of drugs is evaluated to determine whether different formulations would allow the same amount of active ingredient and efficacy in the body. Bioavailability of drugs is assessed to understand what percentage of a drug gets in the systemic circulation when given through non-intravenous routes of administration (e.g., orally). These studies are essential to appraise the efficacy and quality of the new drug products.
Companies that sell Pharmaceutical Contract Bioequivalence Testing Services
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