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Both food supplements and medical drugs are examined in accordance with a detailed plan. For instance, we test if capsules and tablets dissolve within a specified period of time to ensure that the active ingredients are effectively released and absorbed by the body. Also, we control that size and weight correspond with the specifications. All finished food supplements must, as a minimum, undergo a random-sample control analysis once a year, whereas each individual production batch of medical drugs must undergo a control analysis in order to document that it meets the specifications. |
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