The development of system of professional information about pharmaceuticals: Quo vadis?


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Abstract

The modern technologies provide broad possibilities for acquiring information about pharmaceuticals. However, reliability of this data has no guarantee. The document about pharmaceutical developed by manufacturer and regulatory authorities is taken very often for the source of official information. The quality of content of these documents is criticized by professional community. In the European Union it is taken for trusting the short characteristic of product (SmPC) that is an official source of information about pharmaceutical. The review presents sections of SmPC criticized more often.

About the authors

Renad N. Alyautdin

The Research center of expertise of means of medical application

Email: аlyautdin@expmed.ru
vice-director of the center of expertise of safety of pharmaceuticals 127051, Moscow, Russia

B. K Romanov

The Research center of expertise of means of medical application

127051, Moscow, Russia

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