It was at least partly because clinical observations led to the conclusion that different specimens of digitalis varied in their potency that the need for assay of the drug was realized. It would seem natural, therefore, to suppose that much attention would have been given to the clinical standardization of digitalis. In an exact sense, however, this is not the case. The problem is, indeed, a difficult one. It is necessary to know the rate of absorption of digitalis, and desirable to know its fate and its rate of elimination. The rates of absorption and elimination of some preparations have been worked out, though not in any large series or with great accuracy; the results show considerable variation from person to person, so that the averages reached stand for a wide range in a relatively small group of cases.