The X-ray fluorescence technique, induced by radioisotopic sources, provides a very simple method for the simultaneous analysis of trace elements in biological samples. For blood, serum, platelets, etc., samples of about 0.1 ml were deposited on filter paper disks, dried, and analyzed. In such a way the "thin specimen" approximation is realized, resulting in the following advantages: The X-ray intensity of a given element is a liner function of mass per unit area over several orders of magnitude. Interelement effects became negligible. The ratio of fluorescent X-rays to scattered radiation is increased. The sensitivity of the technique for elements with atomic number ranging from about 20-92 varies from some units to some tens of parts per million by weight in 100 s measuring time, by using a gas proportional counter, and from about some tenths to some parts per million by using an X-ray semiconductor detector, in a measuring time of 10(3)-10(4)s. In such a way and with the described features, the Cl, K, Ca, Fe, Cu, Zn, Br content of several speciments of blood and serum was determined. Measurements were further carried out in order to labelling blood components with stable tracers and to detect their concentration by means of the X-ray fluorescence technique. The life span of platelets was, for example, measured after labelling platelets with stable Selenocystine. The sensitivity of the XRF technique can further be enhanced by about three orders of magnitude by using a pre-enrichment step with ion-exchange resins and liquid volumes not lower than 500 ml. Urine analyses have been carried in such a way, and copper in about 20 ml serum after selective extraction.