Abstract
The regulations of the law for medical products have to be followed when medical products are put on the market or into service or when medical products are operated. On January, 1st, 1995 the law for medical products came into force, and the corresponding terms of the X-ray and radiation protection regulations were adapted. The present paper deals with the effects of the law for medical products upon the operators, manufacturers and suppliers of equipment subjected to the X-ray and radiation protection regulations. The impact upon the boards and the authorities as well as the experts is also discussed. Similar adaptions have been necessary in Austria since the Board's guidelines concerning medical products had to be included into national law, too. Switzerland, however, not being a member of the European Union, is not obliged to follow these regulations, although the essential proposals of these guidelines for medical products have also influenced the law in Switzerland.
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