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Medicinal Product

IN THE EUROPEAN UNION A “MEDICINAL PRODUCT” IS DEFINED AS FOLLOWS:

(a) Any substance or combination of substances presented as having properties for treating or preventing a disease in human beings; or

(b) Any substance or combination of substances which may be used in or administered to human beings either with a view to restoring, correcting or modifying physiological functions by exerting a pharmacological, immunological or metabolic action, or to making a medical diagnosis.’”