Substandard And Counterfeit Medicines Scientific Journals
There is no clear and agreed international definition of counterfeit drugs. It defines a fake drug as an unintentionally and fraudulently misidentified drug in relation to identity and / or origin. Counterfeiting can apply to generic and branded products. Counterfeit products may include the following: the wrong ingredients, the right ingredients, no active ingredients, fake packaging or insufficient materials. Sub-standard
drugs are defined as original
drugs that failed to pass the quality measurements and prescribed devices. These quality standards tests were derived from the pharmaceutical drugs. In 2011, WHO member states chose to include counterfeit and substandard
drugs under the new term 'false, nonstandard medical products with the wrong, fake, counterfeit label'.
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